Tricyclic quinoline and quinoxaline derivatives

ABSTRACT

The present invention relates to tricyclic quinoline and quinoxaline derivatives, to a pharmaceutical composition containing such compounds, to their use as modulators, especially agonists or partial agonists, of the 5-HT2C receptor, their use for preparing a medicament for the prevention or treatment of conditions and disorders which respond to the modulation of 5-HT2C receptor, and to a method for preventing or treating conditions and disorders which respond to the modulation of 5-HT2C receptor.

CROSS-REFERENCE TO RELATED APPLICATIONS

This is a non-provisional of U.S. Patent Application No. 61/701,514, filed on Sep. 14, 2012, U.S. Patent Application No. 61/701,531, filed on Sep. 14, 2012, U.S. Patent Application No. 61/793,033, filed on Mar. 15, 2013, and claims priority to Chinese Patent Application No. CN 201310410951.1, filed on Sep. 11, 2013, the contents of all of which are fully incorporated herein by reference.

FIELD OF THE INVENTION

The present invention relates to tricyclic quinoline and quinoxaline derivatives, to a pharmaceutical composition containing such compounds, to their use as modulators, especially agonists or partial agonists, of the 5-HT_(2C) receptor, their use for preparing a medicament for the prevention or treatment of conditions and disorders which respond to the modulation of 5-HT_(2C) receptor, to a method for preventing or treating conditions and disorders which respond to the modulation of 5-HT_(2C) receptor, and processes for preparing such compounds and compositions.

BACKGROUND OF THE INVENTION

Diseases, disorders and conditions where 5-HT_(2C) modulation is desired are for example depression, anxiety, schizophrenia, bipolar disorder, obsessive compulsive disorder, migraine, pain, epilepsy, substance abuse, eating disorders, obesity, diabetes, erectile dysfunction and others.

Serotonin (5-hydroxytryptamine, 5-HT), a monoamine neurotransmitter and local hormone, is formed by the hydroxylation and decarboxylation of tryptophan. The greatest concentration is found in the enterochromaffin cells of the gastrointestinal tract, the remainder being predominantly present in platelets and in the Central Nervous System (CNS). 5-HT is implicated in a vast array of physiological and pathophysiological pathways. In the periphery, it contracts a number of smooth muscles and induces endothelium-dependent vasodilation. In the CNS, it is believed to be involved in a wide range of functions, including the control of appetite, mood, anxiety, hallucinations, sleep, vomiting and pain perception.

Neurons that secrete 5-HT are termed serotonergic. The function of 5-HT is exerted upon its interaction with specific (serotonergic) neurons. Seven types of 5-HT receptors have been identified: 5-HT₁ (with subtypes 5-HT_(1A), 5-HT_(1B), 5-HT_(1D), 5-HT_(1E) and 5-HT_(1F)), 5-HT₂ (with subtypes 5-HT_(2A), 5-HT_(2B) and 5-HT₂c), 5-HT₃, 5-HT₄, 5-HT₅ (with subtypes 5-HT_(5A) and 5-HT_(5B)), 5-HT₆ and 5-HT₇. Most of these receptors are coupled to G-proteins that affect the activities of adenylate cyclase or phospholipase Cγ.

Alterations in the activity of multiple neurotransmitter receptor systems (dopamine, serotonin, glutamate, GABA, acetylcholine) have been implicated in the manifestation of the symptoms of schizophrenia. The most widely accepted “Dopamine Hypothesis of Schizophrenia” in its simplest form states that the positive symptoms of this pathology relate to a functional hyperactivity of the mesolimbic dopaminergic system, while the negative and cognitive aspects can be traced to a functional hypoactivity of the mesocortical dopaminergic projections. Atypical antipsychotics block the mesolimbic dopaminergic neurotransmission, thereby controlling positive symptoms, with little or no effect on the nigrostriatal system, leading to less induction of extrapyramidal side effects (EPS).

Primary negative and cognitive symptoms of schizophrenia reflect a dysfunction of the frontal cortex (“hypofrontality”), which is thought to be induced by a decreased tone in the mesocortical dopaminergic projection field [Davis K L, Kahn R S, Ko G and Davidson M (1991). Dopamine in schizophrenia: a review and re-conceptualization. Am J Psychiatry 148: 1474-86. Weinberger D R and Berman K F (1996). Prefrontal function in schizophrenia: confounds and controversies. Philos Trans R Soc Lond B Biol Sci 351: 1495-503]. Agents that selectively enhance dopamine levels in the cortex have the potential to address the negative symptoms of this disorder. Atypical antipsychotics lack robust efficacy against negative and cognitive components of the schizophrenic syndrome.

The schizophrenic symptomatology is further complicated by the occurrence of drug-induced so-called secondary negative symptoms and cognitive impairment, which are difficult to distinguish from primary negative and cognitive symptoms [Remington G and Kapur S (2000). Atypical antipsychotics: are some more atypical than others?Psychopharmacol 148: 3-15]. The occurrence of secondary negative symptoms not only limits therapeutic efficacy but also, together with these side effects, negatively affects patient compliance.

It may thus be hypothesized that a novel mechanistic approach that blocks dopaminergic neurotransmission in the limbic system but does not affect the striatal and pituitary projection fields, and stimulates frontocortical projection fields, would provide an efficacious treatment for all parts of the schizophrenic pathology, including its positive, negative and cognitive symptoms. Moreover, a selective compound that is substantially free of the ancillary pharmacology that characterizes current agents would be expected to avoid a variety of off-target side effects that plague current treatments such as extrapyramidal side effects (EPS) and weight gain.

The 5-HT_(2C) receptor, previously named 5-HT1C, is a G-protein-coupled receptor, which couples to multiple cellular effector systems including the phospholipase C, A and D pathways. It is found primarily in the brain and its distribution is particularly high in the plexus choroideus, where it is assumed to control cerebrospinal fluid production [Kaufman M J, Hirata F (1996) Cyclic GMP inhibits phosphoinositide turnover in choroid plexus: evidence for interactions between second messengers concurrently triggered by 5-HT_(2C) receptors. Neurosci Lett 206:153-156]. Very high levels were also found in the retrosplenial, piriform and entorhinal cortex, anterior olfactory nucleus, lateral septal nucleus, subthalamic nucleus, amygdala, subiculum and ventral part of CA3, lateral habenula, substantia nigra pars compacta, several brainstem nuclei and the whole grey matter of the spinal cord [Pompeiano M, Palacios J M, Mengod G (1994). Distribution of the serotonin 5-HT2 receptor family mRNAs: comparison between 5-HT_(2A) and 5-HT_(2C) receptors. Brain Res Mol Brain Res 23:163-178]. A comparison of the distribution of 5-HT_(2C) mRNA with that of 5-HT₂c protein in monkey and human brains has revealed both pre- and postsynaptic localization [Lopez-Gimenez J F, Mengod G, Palacios J M, Vilaro M T (2001) Regional distribution and cellular localization of 5-HT_(2C) receptor mRNA in monkey brain: comparison with [³H]mesulergine binding sites and choline acetyltransferase mRNA. Synapse 42:12-26].

It is anticipated that modulation of the 5-HT_(2C) receptor will improve disorders such as depression, anxiety, schizophrenia, cognitive deficits of schizophrenia, obsessive compulsive disorder, bipolar disorder, migraine, epilepsy, substance abuse, eating disorders, obesity, diabetes, sexual dysfunction/erectile dysfunction, sleep disorders, psoriasis, Parkinson's disease, pain conditions and disorders, and spinal cord injury, smoking cessation, ocular hypertension and Alzheimer's disease. Modulators of the 5-HT_(2C) receptor are also shown to be useful in the modulation of bladder function, including the prevention or treatment of urinary incontinence.

There is an ongoing need for providing compounds having high affinity and selectivity for the 5-HT_(2c) receptor. In particular the compounds should have low affinity to adrenergic receptors, such as the al-adrenergic receptor, histamine receptors, such as the H₁-receptor, and dopaminergic receptors, such as the D₂-receptor, in order to avoid or reduce side effects associated with modulation of these receptors, such as postural hypotension, reflex tachycardia, potentiation of the antihypertensive effect of prazosin, terazosin, doxazosin and labetalol or dizziness associated with the blockade of the α₁-adrenergic receptor, weight gain, sedation, drowsiness or potentiation of central depressant drugs associated with the blockade of the H₁-receptor, or extrapyramidal movement disorder, such as dystonia, parkinsonism, akathisia, tardive dyskinesia or rabbit syndrome, or endocrine effects, such as prolactin elevation (galactorrhea, gynecomastia, mentstrual changes, sexual dysfunction in males), associated with the blockade of the D₂-receptor.

The present invention provides compounds which have an affinity for the 5-HT_(2C), thus allowing the treatment of disorders related to or affected by the 5-HT_(2C) receptor.

SUMMARY OF THE INVENTION

The invention is directed to tricyclic quinoline and quinoxaline derivatives, compositions comprising such compounds, their use as modulators, especially agonists or partial agonists, of the 5-HT_(2C) receptor, their use for preparing a medicament for the prevention or treatment of conditions and disorders which respond to the modulation of 5-HT_(2C) receptor, to a method for preventing or treating conditions and disorders which respond to the modulation of 5-HT_(2C) receptor, and processes for preparing such compounds and compositions.

In one aspect, the present invention relates to compounds of the formula (I):

wherein

-   G is (CR^(3a)R^(3b))_(n); -   X is NR⁶ or CR⁷R⁸; -   R¹ is selected from the group consisting of hydrogen, cyano,     C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, —C(═O)R¹⁰, phenyl, phenyl-C₁-C₂-alkyl and     a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated     or maximally unsaturated heterocyclic ring containing 1, 2, 3 or 4     heteroatoms or heteroatom groups independently selected from N, O,     S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups     as ring members, where the cyclic moieties in the three     last-mentioned radicals may be substituted with one or more     substituents R¹¹; -   each R² is independently selected from the group consisting of     cyano, nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl,     C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl,     fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy,     C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated     C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     -   —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),         C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy,         phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy         and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring containing 1, 2, 3 or         4 heteroatoms or heteroatom groups independently selected from         N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the         cyclic moieties in the six last-mentioned radicals may be         substituted with one or more substituents R¹¹; -   R^(3a) and R^(3b), independently of each other, are selected from     the group consisting of hydrogen, cyano, nitro, C₁-C₆-alkyl,     fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl,     fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     -   —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),         C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy,         phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy         and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring containing 1, 2, 3 or         4 heteroatoms or heteroatom groups independently selected from         N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the         cyclic moieties in the six last-mentioned radicals may be         substituted with one or more substituents R¹¹; -   R^(4a) and R^(4b), independently of each other, are selected from     the group consisting of hydrogen, cyano, nitro, C₁-C₆-alkyl,     fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl,     fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl,     -   —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), —NR^(12a)C(O)R¹⁰,         —C(═O)R¹⁰, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy,         fluorinated C₁-C₆-alkylcarbonyloxy, phenyl, phenyl-C₁-C₂-alkyl,         phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-, 5-, 6-, 7- or         8-membered saturated, partially unsaturated or maximally         unsaturated ring containing 1, 2, 3 or 4 heteroatoms or         heteroatom groups independently selected from N, O, S, NO, SO,         SO₂, C═O and C═S as ring members, where the cyclic moieties in         the six last-mentioned radicals may be substituted with one or         more substituents R¹¹; or     -   R^(4a) and R^(4b) form together a group ═O or ═S; -   R^(5a) and R^(5b), independently of each other, are selected from     the group consisting of hydrogen, deuterium, halogen, cyano, nitro,     hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl,     C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated     C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,     C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-,     5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or     heteroatom groups independently selected from N, O, S, NO, SO, SO₂,     C═O and C═S as ring members, where the cyclic moieties in the six     last-mentioned radicals may be substituted with one or more     substituents R¹¹; where R^(5a) and R^(5b) are not simultaneously     hydroxy; or     -   R^(5a) and R^(5b), together with the carbon atom they are bound         to, form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring (i.e. a spiro ring),         where the ring may contain 1, 2, 3 or 4 heteroatoms or         heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O         and C═S as ring members, and where the ring may be substituted         with one or more substituents R¹¹; or     -   R^(5a) and R⁶, together with the atoms they are bound to, form a         3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated heterocyclic ring, where         the ring may further contain 1, 2, 3 or 4 heteroatoms or         heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O         and C═S as ring members, and where the ring may be substituted         with one or more substituents R¹¹; or     -   R^(5a) and R⁷, together with the carbon atoms they are bound to,         form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring, where the ring may         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         R¹¹; -   R⁶ is selected from the group consisting of hydrogen, cyano,     C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,     C₃-C₈-cycloalkyl-C₁-C₄-alkyl, fluorinated     C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₁-C₆-alkoxy, fluorinated,     C₁-C₆-alkoxy, —C(═O)R¹⁰, —SO₂R¹⁰, phenyl, phenyl-C₁-C₂-alkyl and a     3-, 4-, 5-, 6-7- or 8-membered saturated, partially unsaturated or     maximally unsaturated heterocyclic ring containing 1, 2, 3 or 4     heteroatoms or heteroatom groups independently selected from N, O,     S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups     as ring members, where the cyclic moieties in the three     last-mentioned radicals may be substituted with one or more     substituents R¹¹; -   R⁷ and R⁸, independently of each other, are selected from the group     consisting of deuterium, halogen, cyano, nitro, hydroxyl,     C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl,     C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated     C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,     C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-,     5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or     heteroatom groups independently selected from N, O, S, NO, SO, SO₂,     C═O and C═S as ring members, where the cyclic moieties in the six     last-mentioned radicals may be substituted with one or more     substituents R¹¹; where R⁷ and R⁸ are not simultaneously hydroxyl;     and where R⁷ is not hydroxyl if R⁸ is C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy,     phenoxy or benzyloxy; or     -   R⁷ and R⁸, together with the carbon atom they are bound to, form         a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring (i.e. a spiro ring),         where the ring may contain 1, 2, 3 or 4 heteroatoms or         heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O         and C═S as ring members, and where the ring may be substituted         with one or more substituents R¹¹;     -   each R⁹ is independently selected from the group consisting of         halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated         C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated         C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,         C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,         C₃-C₈-cycloalkenyl, fluorinated C₃-C₈-cycloalkenyl,         C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy,         C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy,         C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated         C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated         C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated         C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),         —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),         C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy,         phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy         and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring containing 1, 2, 3 or         4 heteroatoms or heteroatom groups independently selected from         N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the         cyclic moieties in the six last-mentioned radicals may be         substituted with one or more substituents R¹¹; or     -   two radicals R⁹ bound on neighbouring carbon atoms, together         with the carbon atoms they are bound to, form a 3-, 4-, 5-, 6-,         7- or 8-membered partially unsaturated or maximally unsaturated         ring, where the ring may contain 1, 2, 3 or 4 heteroatoms or         heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O         and C═S as ring members, and where the ring may be substituted         with one or more substituents R¹¹; -   each R¹⁰ is independently selected from the group consisting of     hydrogen, cyano, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl,     C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl,     fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, benzyloxy and a 3-, 4-, 5-, 6-, 7- or     8-membered saturated, partially unsaturated or maximally unsaturated     ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups     independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as     ring members, where the cyclic moieties in the five last-mentioned     radicals may be substituted with one or more substituents R¹¹; -   each R¹¹ is independently selected from the group consisting of     halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —COOH, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyl, fluorinated C₁-C₆-alkylcarbonyl,     C₁-C₆-alkoxycarbonyl, fluorinated C₁-C₆-alkoxycarbonyl,     SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy and fluorinated     C₁-C₆-alkylcarbonyloxy;     -   or two radicals R¹¹, together with the atom(s) they are bound         to, form a saturated, partially unsaturated or maximally         unsaturated 3-, 4-, 5-, 6- or 7-membered carbocyclic or         heterocyclic ring, where the heterocyclic ring contains 1, 2 or         3 heteroatoms or heteroatom groups independently selected from         N, O, S, NO, SO, SO₂, C═O and C═S as ring members; -   R^(12a) and R^(12b), independently of each other and independently     of each occurrence, are selected from the group consisting of     hydrogen, cyano, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated     C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,     C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyl,     fluorinated C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, fluorinated     C₁-C₆-alkoxycarbonyl, phenyl and benzyl, where the phenyl moieties     in the two last-mentioned radicals may carry 1, 2 or 3 substituents     selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy; or,     -   if R^(12a) and R^(12b) are bound to the same nitrogen atom,         together with this nitrogen atom may form a 3-, 4-, 5-, 6-, 7-         or 8-membered saturated, partially unsaturated or maximally         unsaturated heterocyclic ring, where the ring may further         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated         C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy; -   a is 0, 1 or 2; -   b is 0, 1, 2 or 3; and -   n is 1 or 2; -   and the N-oxides, tautomeric forms, stereoisomers and     pharmaceutically acceptable salts thereof, and the compound of the     general formula I, wherein at least one of the atoms has been     replaced by its stable, non-radioactive isotope.

In another aspect, the invention relates to compounds of formula I as defined above, wherein

-   G is (CR^(3a)R^(3b))_(n); -   X is NR⁶ or CR⁷R⁸; -   R¹ is selected from the group consisting of hydrogen, cyano,     C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, —C(═O)R¹⁰, phenyl, phenyl-C₁-C₂-alkyl and     a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated     or maximally unsaturated heterocyclic ring containing 1, 2, 3 or 4     heteroatoms or heteroatom groups independently selected from N, O,     S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups     as ring members, where the cyclic moieties in the three     last-mentioned radicals may be substituted with one or more     substituents R¹¹; -   each R² is independently selected from the group consisting of     cyano, nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl,     C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl,     fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy,     C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated     C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(2a)R^(12b), —CH₂NR^(12a)R^(12b),     -   —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),         C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy,         phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy         and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring containing 1, 2, 3 or         4 heteroatoms or heteroatom groups independently selected from         N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the         cyclic moieties in the six last-mentioned radicals may be         substituted with one or more substituents R¹¹; -   R^(3a) and R^(3b), independently of each other, are selected from     the group consisting of hydrogen, cyano, nitro, C₁-C₆-alkyl,     fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl,     fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     -   —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),         C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy,         phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy         and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring containing 1, 2, 3 or         4 heteroatoms or heteroatom groups independently selected from         N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the         cyclic moieties in the six last-mentioned radicals may be         substituted with one or more substituents R¹¹; -   R^(4a) and R^(4b), independently of each other, are selected from     the group consisting of hydrogen, cyano, nitro, C₁-C₆-alkyl,     fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl,     fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl,     -   —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), —NR^(12a)C(O)R¹⁰,         —C(═O)R¹⁰, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy,         fluorinated C₁-C₆-alkylcarbonyloxy, phenyl, phenyl-C₁-C₂-alkyl,         phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-, 5-, 6-, 7- or         8-membered saturated, partially unsaturated or maximally         unsaturated ring containing 1, 2, 3 or 4 heteroatoms or         heteroatom groups independently selected from N, O, S, NO, SO,         SO₂, C═O and C═S as ring members, where the cyclic moieties in         the six last-mentioned radicals may be substituted with one or         more substituents R¹¹; or     -   R^(4a) and R^(4b) form together a group ═O or ═S; -   R^(5a) and R^(5b), independently of each other, are selected from     the group consisting of hydrogen, deuterium, halogen, cyano, nitro,     hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl,     C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated     C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,     C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-,     5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or     heteroatom groups independently selected from N, O, S, NO, SO, SO₂,     C═O and C═S as ring members, where the cyclic moieties in the six     last-mentioned radicals may be substituted with one or more     substituents R¹¹; or     -   R^(5a) and R^(5b), together with the carbon atom they are bound         to, form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring, where the ring may         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         R¹¹; or     -   R^(5a) and R⁶, together with the atoms they are bound to, form a         3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated heterocyclic ring, where         the ring may further contain 1, 2, 3 or 4 heteroatoms or         heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O         and C═S as ring members, and where the ring may be substituted         with one or more substituents R¹¹; or     -   R^(5a) and R⁷, together with the carbon atoms they are bound to,         form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring, where the ring may         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         R¹¹; -   R⁶ is selected from the group consisting of hydrogen, cyano,     C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,     C₃-C₈-cycloalkyl-C₁-C₄-alkyl, fluorinated     C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, —C(═O)R¹⁰, —SO₂R¹⁰, phenyl, phenyl-C₁-C₂-alkyl and a     3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated heterocyclic ring containing 1, 2, 3 or 4     heteroatoms or heteroatom groups independently selected from N, O,     S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups     as ring members, where the cyclic moieties in the three     last-mentioned radicals may be substituted with one or more     substituents R¹¹; -   R⁷ and R⁸, independently of each other, are selected from the group     consisting of deuterium, halogen, cyano, nitro, C₁-C₆-alkyl,     fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl,     fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-,     5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or     heteroatom groups independently selected from N, O, S, NO, SO, SO₂,     C═O and C═S as ring members, where the cyclic moieties in the six     last-mentioned radicals may be substituted with one or more     substituents R¹¹; or     -   R⁷ and R⁸, together with the carbon atom they are bound to, form         a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring, where the ring may         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         R¹¹; -   each R⁹ is independently selected from the group consisting of     halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl,     fluorinated C₃-C₈-cycloalkenyl, C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy,     C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated     C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-,     5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or     heteroatom groups independently selected from N, O, S, NO, SO, SO₂,     C═O and C═S as ring members, where the cyclic moieties in the six     last-mentioned radicals may be substituted with one or more     substituents R¹¹; or     -   two radicals R⁹ bound on neighbouring carbon atoms, together         with the carbon atoms they are bound to, form a 3-, 4-, 5-, 6-,         7- or 8-membered partially unsaturated or maximally unsaturated         ring, where the ring may contain 1, 2, 3 or 4 heteroatoms or         heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O         and C═S as ring members, and where the ring may be substituted         with one or more substituents R¹¹; -   each R¹⁰ is independently selected from the group consisting of     hydrogen, cyano, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl,     C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl,     fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, benzyloxy and a 3-, 4-, 5-, 6-, 7- or     8-membered saturated, partially unsaturated or maximally unsaturated     ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups     independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as     ring members, where the cyclic moieties in the five last-mentioned     radicals may be substituted with one or more substituents R¹¹; -   each R¹¹ is independently selected from the group consisting of     halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —COOH, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyl, fluorinated C₁-C₆-alkylcarbonyl,     C₁-C₆-alkoxycarbonyl, fluorinated C₁-C₆-alkoxycarbonyl,     SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy and fluorinated     C₁-C₆-alkylcarbonyloxy; -   R^(12a) and R^(12b), independently of each other and independently     of each occurrence, are selected from the group consisting of     hydrogen, cyano, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated     C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,     C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyl,     fluorinated C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, fluorinated     C₁-C₆-alkoxycarbonyl, phenyl and benzyl, where the phenyl moieties     in the two last-mentioned radicals may carry 1, 2 or 3 substituents     selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy; or,     -   if R^(12a) and R^(12b) are bound to the same nitrogen atom,         together with this nitrogen atom may form a 3-, 4-, 5-, 6-, 7-         or 8-membered saturated, partially unsaturated or maximally         unsaturated heterocyclic ring, where the ring may further         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated         C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy; -   a is 0, 1 or 2; -   b is 0, 1, 2 or 3; and -   n is 1 or 2; -   and the N-oxides, tautomeric forms, stereoisomers and     pharmaceutically acceptable salts thereof, and the compound of the     general formula I, wherein at least one of the atoms has been     replaced by its stable, non-radioactive isotope.

Preferably, R^(5a) and R^(5b) are not simultaneously hydroxyl.

In another aspect, the invention relates to compounds of formula I

wherein

-   G is (CR^(3a)R^(3b))_(n); -   X is NR⁶ or CR⁷R⁸; -   R¹ is selected from the group consisting of hydrogen, cyano,     C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, —C(═O)R¹⁰, phenyl, phenyl-C₁-C₂-alkyl and     a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated     or maximally unsaturated heterocyclic ring containing 1, 2, 3 or 4     heteroatoms or heteroatom groups independently selected from N, O,     S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups     as ring members, where the cyclic moieties in the three     last-mentioned radicals may be substituted with one or more     substituents R¹¹; -   each R² is independently selected from the group consisting of     cyano, nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl,     C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl,     fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy,     C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated     C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     -   —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),         C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy,         phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy         and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring containing 1, 2, 3 or         4 heteroatoms or heteroatom groups independently selected from         N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the         cyclic moieties in the six last-mentioned radicals may be         substituted with one or more substituents R¹¹; -   R^(3a) and R^(3b), independently of each other, are selected from     the group consisting of hydrogen, cyano, nitro, C₁-C₆-alkyl,     fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl,     fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     -   —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),         C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy,         phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy         and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring containing 1, 2, 3 or         4 heteroatoms or heteroatom groups independently selected from         N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the         cyclic moieties in the six last-mentioned radicals may be         substituted with one or more substituents R¹¹; -   R^(4a) and R^(4b), independently of each other, are selected from     the group consisting of hydrogen, cyano, nitro, C₁-C₆-alkyl,     fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl,     fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl,     -   —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), —NR^(12a)C(O)R¹⁰,         —C(═O)R¹⁰, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy,         fluorinated C₁-C₆-alkylcarbonyloxy, phenyl, phenyl-C₁-C₂-alkyl,         phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-, 5-, 6-, 7- or         8-membered saturated, partially unsaturated or maximally         unsaturated ring containing 1, 2, 3 or 4 heteroatoms or         heteroatom groups independently selected from N, O, S, NO, SO,         SO₂, C═O and C═S as ring members, where the cyclic moieties in         the six last-mentioned radicals may be substituted with one or         more substituents R¹¹; or R^(4a) and R^(4b) form together a         group ═O or ═S; -   R^(5a) and R^(5b), independently of each other, are selected from     the group consisting of hydrogen, deuterium, halogen, cyano, nitro,     hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl,     C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated     C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,     C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-,     5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or     heteroatom groups independently selected from N, O, S, NO, SO, SO₂,     C═O and C═S as ring members, where the cyclic moieties in the six     last-mentioned radicals may be substituted with one or more     substituents R¹¹; or     -   R^(5a) and R^(5b), together with the carbon atom they are bound         to, form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring, where the ring may         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         R¹¹; or     -   R^(5a) and R⁶, together with the atoms they are bound to, form a         3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated heterocyclic ring, where         the ring may further contain 1, 2, 3 or 4 heteroatoms or         heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O         and C═S as ring members, and where the ring may be substituted         with one or more substituents R¹¹; or     -   R^(5a) and R⁷, together with the carbon atoms they are bound to,         form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring, where the ring may         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         R¹¹; -   R⁶ is selected from the group consisting of hydrogen, cyano,     C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, —C(═O)R¹⁰, —SO₂R¹⁰, phenyl,     phenyl-C₁-C₂-alkyl and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated,     partially unsaturated or maximally unsaturated heterocyclic ring     containing 1, 2, 3 or 4 heteroatoms or heteroatom groups     independently selected from N, O, S, NO, SO and SO₂ and optionally     also 1 or 2 C═O and/or C═S groups as ring members, where the cyclic     moieties in the three last-mentioned radicals may be substituted     with one or more substituents R¹¹; -   R⁷ and R⁸, independently of each other, are selected from the group     consisting of deuterium, halogen, cyano, nitro, C₁-C₆-alkyl,     fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl,     fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-,     5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or     heteroatom groups independently selected from N, O, S, NO, SO, SO₂,     C═O and C═S as ring members, where the cyclic moieties in the six     last-mentioned radicals may be substituted with one or more     substituents R¹¹; or     -   R⁷ and R⁸, together with the carbon atom they are bound to, form         a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring, where the ring may         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         R¹¹; -   each R⁹ is independently selected from the group consisting of     halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl,     fluorinated C₃-C₈-cycloalkenyl, C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy,     C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated     C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-,     5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or     heteroatom groups independently selected from N, O, S, NO, SO, SO₂,     C═O and C═S as ring members, where the cyclic moieties in the six     last-mentioned radicals may be substituted with one or more     substituents R¹¹; or     -   two radicals R⁹ bound on neighbouring carbon atoms, together         with the carbon atoms they are bound to, form a 3-, 4-, 5-, 6-,         7- or 8-membered partially unsaturated or maximally unsaturated         ring, where the ring may contain 1, 2, 3 or 4 heteroatoms or         heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O         and C═S as ring members, and where the ring may be substituted         with one or more substituents R¹¹; -   each R¹⁰ is independently selected from the group consisting of     hydrogen, cyano, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl,     C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl,     fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated     C₁-C₆-alkoxy, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), phenyl,     phenyl-C₁-C₂-alkyl, phenoxy, benzyloxy and a 3-, 4-, 5-, 6-, 7- or     8-membered saturated, partially unsaturated or maximally unsaturated     ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups     independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as     ring members, where the cyclic moieties in the five last-mentioned     radicals may be substituted with one or more substituents R¹¹; -   each R¹¹ is independently selected from the group consisting of     halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —COOH, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     C₁-C₆-alkylcarbonyl, fluorinated C₁-C₆-alkylcarbonyl,     C₁-C₆-alkoxycarbonyl, fluorinated C₁-C₆-alkoxycarbonyl,     SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy and fluorinated     C₁-C₆-alkylcarbonyloxy; -   R^(12a) and R^(12b), independently of each other and independently     of each occurrence, are selected from the group consisting of     hydrogen, cyano, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated     C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl,     C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyl,     fluorinated C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, fluorinated     C₁-C₆-alkoxycarbonyl, phenyl and benzyl, where the phenyl moieties     in the two last-mentioned radicals may carry 1, 2 or 3 substituents     selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy; or,     -   if R^(12a) and R^(12b) are bound to the same nitrogen atom,         together with this nitrogen atom may form a 3-, 4-, 5-, 6-, 7-         or 8-membered saturated, partially unsaturated or maximally         unsaturated heterocyclic ring, where the ring may further         contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups         selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and         where the ring may be substituted with one or more substituents         selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated         C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy; -   a is 0, 1 or 2; -   b is 0, 1, 2 or 3; and -   n is 1 or 2;     and the N-oxides, tautomeric forms, stereoisomers and     pharmaceutically acceptable salts thereof, and the compound of the     general formula I, wherein at least one of the atoms has been     replaced by its stable, non-radioactive isotope.

Preferably, R^(5a) and R^(5b) are not simultaneously hydroxyl.

In another aspect, the invention relates to a pharmaceutical composition comprising a therapeutically effective amount of at least one compound of formula I or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof, or comprising at least one compound as defined above or below wherein at least one of the atoms has been replaced by its stable, non-radioactive isotope, preferably wherein at least one hydrogen atom has been replaced by a deuterium atom, in combination with at least one pharmaceutically acceptable carrier and/or auxiliary substance.

In yet another aspect, the invention relates to a compound of formula I or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for use as a medicament.

In yet another aspect, the invention relates to a compound of formula I or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for the treatment of disorders which responds to the modulation of the 5-HT_(2c) receptor.

In yet another aspect, the invention relates to the use of a compound of formula I or of an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for the manufacture of a medicament for the treatment of disorders which respond to the modulation of the 5-HT_(2c) receptor.

In yet another aspect, the invention relates to the use of a compound of formula I or of an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for the manufacture of a medicament for the treatment of disorders selected from the group consisting of damage of the central nervous system, disorders of the central nervous system, eating disorders, ocular hypertension, cardiovascular disorders, gastrointestinal disorders and diabetes, and especially from the group consisting of bipolar disorder, depression, atypical depression, mood episodes, adjustment disorders, anxiety, panic disorders, post-traumatic syndrome, psychoses, schizophrenia, cognitive deficits of schizophrenia, memory loss, dementia of aging, Alzheimer's disease, behavioral disorders associated with dementia, social phobia, mental disorders in childhood, attention deficit hyperactivity disorder, organic mental disorders, autism, mutism, disruptive behavior disorder, impulse control disorder, borderline personality disorder, obsessive compulsive disorder, migraine and other conditions associated with cephalic pain or other pain, raised intracranial pressure, seizure disorders, epilepsy, substance use disorders, alcohol abuse, cocaine abuse, tobacco abuse, smoking cessation, sexual dysfunction/erectile dysfunction in males, sexual dysfunction in females, premenstrual syndrome, late luteal phase syndrome, chronic fatigue syndrome, sleep disorders, sleep apnoea, chronic fatigue syndrome, psoriasis, Parkinson's disease, spinal cord injury, trauma, stroke, pain, bladder dysfunction/urinary incontinence, encephalitis, meningitis, eating disorders, obesity, bulimia, weight loss, anorexia nervosa, ocular hypertension, cardiovascular disorders, gastrointestinal disorders, diabetes insipidus, diabetes mellitus, type I diabetes, type II diabetes, type III diabetes, diabetes secondary to pancreatic diseases, diabetes related to steroid use, diabetes complications, hyperglycemia and insulin resistance.

In yet another aspect, the invention relates to a method for treating disorders which respond to the modulation of the 5-HT_(2c) receptor, which method comprises administering to a subject in need thereof at least one compound of formula I or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof.

In yet another aspect, the invention relates to a method for treating disorders selected from the group consisting of damage of the central nervous system, disorders of the central nervous system, eating disorders, ocular hypertension, cardiovascular disorders, gastrointestinal disorders and diabetes, and especially from the group consisting of bipolar disorder, depression, atypical depression, mood episodes, adjustment disorders, anxiety, panic disorders, post-traumatic syndrome, psychoses, schizophrenia, cognitive deficits of schizophrenia, memory loss, dementia of aging, Alzheimer's disease, behavioral disorders associated with dementia, social phobia, mental disorders in childhood, attention deficit hyperactivity disorder, organic mental disorders, autism, mutism, disruptive behavior disorder, impulse control disorder, borderline personality disorder, obsessive compulsive disorder, migraine and other conditions associated with cephalic pain or other pain, raised intracranial pressure, seizure disorders, epilepsy, substance use disorders, alcohol abuse, cocaine abuse, tobacco abuse, smoking cessation, sexual dysfunction/erectile dysfunction in males, sexual dysfunction in females, premenstrual syndrome, late luteal phase syndrome, chronic fatigue syndrome, sleep disorders, sleep apnoea, chronic fatigue syndrome, psoriasis, Parkinson's disease, spinal cord injury, trauma, stroke, pain, bladder dysfunction/urinary incontinence, encephalitis, meningitis, eating disorders, obesity, bulimia, weight loss, anorexia nervosa, ocular hypertension, cardiovascular disorders, gastrointestinal disorders, diabetes insipidus, diabetes mellitus, type I diabetes, type II diabetes, type III diabetes, diabetes secondary to pancreatic diseases, diabetes related to steroid use, diabetes complications, hyperglycemia and insulin resistance, which method comprises administering to a subject in need thereof at least one compound of formula I or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof.

DETAILED DESCRIPTION

The compounds of the formula I may exist in different spatial arrangements. For example, if the compounds possess one or more centers of asymmetry, polysubstituted rings or double bonds, or as different tautomers, the present invention contemplates the possible use of enantiomeric mixtures, in particular racemates, diastereomeric mixtures and tautomeric mixtures, such as the respective essentially pure enantiomers, diastereomers and tautomers of the compounds of formula I and/or their salts.

It is likewise possible to use physiologically tolerated salts of the compounds of the formula I, especially acid addition salts with physiologically tolerated acids. Examples of suitable physiologically tolerated organic and inorganic acids are hydrochloric acid, hydrobromic acid, phosphoric acid, sulfuric acid, acetic acid, trifluoroacetic acid, C₁-C₄-alkylsulfonic acids, such as methanesulfonic acid, aromatic sulfonic acids, such as benzenesulfonic acid and toluenesulfonic acid, oxalic acid, maleic acid, fumaric acid, lactic acid, tartaric acid, adipic acid and benzoic acid. Other utilizable acids are described in Fortschritte der Arzneimittelforschung [Advances in drug research], Volume 10, pages 224 et seq., Birkhäuser Verlag, Basel and Stuttgart, 1966.

The compounds of formula I may also be present in the form of tautomers. In one aspect, tautomery may be present in compounds I wherein R^(4a) and R^(4b) form together a group ═O and R^(5a) or R^(5b) is H. For example, the compounds of formula I may have the following tautomeric formulae:

In another aspect, tautomery may be present in compounds I containing rings which have one or more C═O groups as ring members which are neighboured to a CH₂ group.

The organic moieties mentioned in the above definitions of the variables are, like the term halogen, collective terms for individual listings of the individual group members. The prefix C_(n)-C_(m) indicates in each case the possible number of carbon atoms in the group.

The term “halogen” denotes in each case fluorine, bromine, chlorine or iodine. In one aspect, the halogen may be fluorine, chlorine or bromine.

The term “alkyl” as used herein and in the alkyl moieties of alkoxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylcarbonyl, alkoxycarbonyl and the like refers to saturated straight-chain or branched hydrocarbon radicals having 1 to 2 (“C₁-C₂-alkyl”), 1 to 3 (“C₁-C₃-alkyl”), 1 to 4 (“C₁-C₄-alkyl”) or 1 to 6 (“C₁-C₆-alkyl”) carbon atoms. C₁-C₂-Alkyl is methyl or ethyl. C₁-C₃-Alkyl is additionally propyl and isopropyl. C₁-C₄-Alkyl is additionally butyl, 1-methylpropyl (sec-butyl), 2-methylpropyl (isobutyl) or 1,1-dimethylethyl (tert-butyl). C₁-C₆-Alkyl is additionally also, for example, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl, 1-ethyl-1-methylpropyl, or 1-ethyl-2-methylpropyl.

The term “fluorinated alkyl” as used herein refers to straight-chain or branched alkyl groups having 1 to 2 (“fluorinated C₁-C₂-alkyl”), 1 to 3 (“fluorinated C₁-C₃-alkyl”), 1 to 4 (“fluorinated C₁-C₄-alkyl”) or 1 to 6 (“fluorinated C₁-C₆-alkyl”) carbon atoms (as mentioned above), where some or all of the hydrogen atoms in these groups are replaced by fluorine atoms. Fluorinated C₁-C₂-alkyl is an alkyl group having 1 or 2 carbon atoms (as mentioned above), where at least one of the hydrogen atoms, e.g. 1, 2, 3, 4 or 5 hydrogen atoms in these groups are replaced by fluorine atoms, such as difluoromethyl, trifluoromethyl, 1-fluoroethyl, (R)-1-fluoroethyl, (S)-1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, or pentafluoroethyl. Fluorinated C₁-C₄-alkyl is a straight-chain or branched alkyl group having 1 to 4 carbon atoms (as mentioned above), where at least one of the hydrogen atoms, e.g. 1, 2, 3, 4 or 5 hydrogen atoms in these groups are replaced by fluorine atoms. Examples are, apart those listed above for C₁-C₂-fluoroalkyl, 1-fluoropropyl, (R)-1-fluoropropyl, (S)-1-fluoropropyl, 2-fluoropropyl, (R)-2-fluoropropyl, (S)-2-fluoropropyl, 3-fluoropropyl, 1,1-difluoropropyl, 2,2-difluoropropyl, 1,2-difluoropropyl, 2,3-difluoropropyl, 1,3-difluoropropyl, 3,3-difluoropropyl, 1,1,2-trifluoropropyl, 1,2,2-trifluoropropyl, 1,2,3-trifluoropropyl, 2,2,3-trifluoropropyl, 3,3,3-trifluoropropyl, 1,1,1-trifluoroprop-2-yl, 2-fluoro-1-methylethyl, (R)-2-fluoro-1-methylethyl, (S)-2-fluoro-1-methylethyl, 2,2-difluoro-1-methylethyl, (R)-2,2-difluoro-1-methylethyl, (S)-2,2-difluoro-1-methylethyl, 1,2-difluoro-1-methylethyl, (R)-1,2-difluoro-1-methylethyl, (S)-1,2-difluoro-1-methylethyl, 2,2,2-trifluoro-1-methylethyl, (R)-2,2,2-trifluoro-1-methylethyl, (S)-2,2,2-trifluoro-1-methylethyl, 2-fluoro-1-(fluoromethyl)ethyl, 1-(difluoromethyl)-2,2-difluoroethyl, 1-(trifluoromethyl)-2,2,2-trifluoroethyl, 1-(trifluoromethyl)-1,2,2,2-tetrafluoroethyl, 1-fluorobutyl, (R)-1-fluorobutyl, (S)-1-fluorobutyl, 2-fluorobutyl, (R)-2-fluorobutyl, (S)-2-fluorobutyl, 3-fluorobutyl, (R)-3-fluorobutyl, (S)-3-fluorobutyl, 4-fluorobutyl, 1,1-difluorobutyl, 2,2-difluorobutyl, 3,3-difluorobutyl, 4,4-difluorobutyl, 4,4,4-trifluorobutyl and the like. Fluorinated C₁-C₆-alkyl is a straight-chain or branched alkyl group having 1 to 6 carbon atoms (as mentioned above), where at least one of the hydrogen atoms, e.g. 1, 2, 3, 4 or 5 hydrogen atoms in these groups are replaced by fluorine atoms. Additionally examples include for C₁-C₄-fluoroalkyl, 1-fluoropentyl, (R)-1-fluoropentyl, (S)-1-fluoropentyl, 2-fluoropentyl, (R)-2-fluoropentyl, (S)-2-fluoropentyl, 3-fluoropentyl, (R)-3-fluoropentyl, (S)-3-fluoropentyl, 4-fluoropentyl, (R)-4-fluoropentyl, (S)-4-fluoropentyl, 5-fluoropentyl, (R)-5-fluoropentyl, (S)-5-fluoropentyl, 1-fluorohexyl, (R)-1-fluorohexyl, (S)-1-fluorohexyl, 2-fluorohexyl, (R)-2-fluorohexyl, (S)-2-fluorohexyl, 3-fluorohexyl, (R)-3-fluorohexyl, (S)-3-fluorohexyl, 4-fluorohexyl, (R)-4-fluorohexyl, (S)-4-fluorohexyl, 5-fluorohexyl, (R)-5-fluorohexyl, (S)-5-fluorohexyl, 6-fluorohexyl, (R)-6-fluorohexyl, (S)-6-fluorohexyl, and the like.

The term “alkenyl” as used herein refers to monounsaturated straight-chain or branched hydrocarbon radicals having 2 to 3 (“C₂-C₃-alkenyl”), 2 to 4 (“C₂-C₄-alkenyl”) or 2 to 6 (“C₂-C₆-alkenyl”) carbon atoms and a double bond in any position, such as C₂-C₃-alkenyl, such as ethenyl, 1-propenyl, 2-propenyl or 1-methylethenyl; C₂-C₄-alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl or 2-methyl-2-propenyl; and C₂-C₆-alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1,1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1,1,2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl, 1-ethyl-2-methyl-2-propenyl and the like.

The term “fluorinated alkenyl” as used herein refers to unsaturated straight-chain or branched hydrocarbon radicals having 2 to 3 (“fluorinated C₂-C₃-alkenyl”), 2 to 4 (“fluorinated C₂-C₄-alkenyl”) or 2 to 6 (“fluorinated C₂-C₆-alkenyl”) carbon atoms and a double bond in any position (as mentioned above), where some or all of the hydrogen atoms in these groups are replaced by fluorine atoms, such as, fluorovinyl, fluoroallyl and the like.

The term “alkynyl” as used herein refers to straight-chain or branched hydrocarbon groups having 2 to 3 (“C₂-C₃-alkynyl”), 2 to 4 (“C₂-C₄-alkynyl”) or 2 to 6 (“C₂-C₆-alkynyl”) carbon atoms and one or two triple bonds in any position, such as C₂-C₃-alkynyl, such as ethynyl, 1-propynyl or 2-propynyl; C₂-C₄-alkynyl, such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl and the like, and C₂-C₆-alkynyl, such as ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl, 3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl, 1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl, 1-ethyl-1-methyl-2-propynyl and the like.

The term “fluorinated alkynyl” as used herein refers to unsaturated straight-chain or branched hydrocarbon radicals having 2 to 3 (“fluorinated C₂-C₃-alkynyl”), 3 to 4 (“fluorinated C₃-C₄-alkynyl”) or 2 to 6 (“fluorinated C₂-C₆-alkynyl”) carbon atoms and one or two triple bonds in any position (as mentioned above), where some or all of the hydrogen atoms in these groups are replaced by fluorine atoms.

The term “cycloalkyl” as used herein refers to mono- or bicyclic saturated hydrocarbon radicals having 3 to 8 (“C₃-C₈-cycloalkyl”), in particular 3 to 6 carbon atoms (“C₃-C₆-cycloalkyl”) or 3 to 5 carbon atoms (“C₃-C₈-cycloalkyl”) or 3 or 4 carbon atoms (“C₃-C₄-cycloalkyl”). In one aspect, C₃-C₄-cycloalkyl, C₃-C₈-cycloalkyl and C₃-C₆-cycloalkyl are monocyclic. Examples for C₃-C₄-cycloalkyl are cyclopropyl and cyclobutyl. Examples of monocyclic radicals having 3 to 5 carbon atoms are cyclopropyl, cyclobutyl and cyclopentyl. Examples of monocyclic radicals having 3 to 6 carbon atoms are cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. Examples of monocyclic radicals having 3 to 8 carbon atoms are cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl. Examples of bicyclic radicals having 7 or 8 carbon atoms comprise bicyclo[2.2.1]heptyl, bicyclo[3.1.1]heptyl, bicyclo[2.2.2]octyl and bicyclo[3.2.1]octyl. In one aspect, the term cycloalkyl denotes a monocyclic saturated hydrocarbon radical.

The term “fluorinated cycloalkyl” as used herein refers to mono- or bicyclic saturated hydrocarbon groups having 3 to 8 (“C₃-C₈-halocycloalkyl”) or preferably 3 to 6 (“C₃-C₆-halocycloalkyl”) or 3 to 5 (“C₃-C₈-halocycloalkyl”) carbon ring members (as mentioned above) in which some or all of the hydrogen atoms are replaced by fluorine atoms. Examples include 1-fluorocyclopropyl, 2-fluorocyclopropyl, (S)- and (R)-2,2-difluorocyclopropyl, 1,2-difluorocyclopropyl, 2,3-difluorocyclopropyl, pentafluorocyclopropyl, 1-fluorocyclobutyl, 2-fluorocyclobutyl, 3-fluorocyclobutyl, 2,2-difluorocyclobutyl, 3,3-difluorocyclobutyl, 1,2-difluorocyclobutyl, 1,3-difluorocyclobutyl, 2,3-difluorocyclobutyl, 2,4-difluorocyclobutyl, 1,2,2-trifluorocyclobutyl, 1-fluorocycloheptyl, 2-fluorocycloheptyl, 3-fluorocycloheptyl, 4-fluorocycloheptyl, 1,2-difluorocycloheptyl, 1,3-difluorocycloheptyl, 1,4-difluorocycloheptyl, 2,2-difluorocycloheptyl, 2,3-difluorocycloheptyl, 2,4-difluorocycloheptyl, 2,5-difluorocycloheptyl, 2,6-difluorocycloheptyl, 2,7-difluorocycloheptyl, 3,3-difluorocycloheptyl, 3,4-difluorocycloheptyl, 3,5-difluorocycloheptyl, 3,6-difluorocycloheptyl, 4,4-difluorocycloheptyl, 4,5-difluorocycloheptyl, and the like.

The term “cycloalkenyl” as used herein refers to monocyclic partially unsaturated, non-aromatic hydrocarbon radicals having 3 to 8 (“C₃-C₈-cycloalkenyl”), in particular 5 to 7 carbon atoms (“C₅-C₇-cycloalkenyl”) or 5 or 6 carbon atoms (“C₅-C₆-cycloalkenyl”) and one or more non-cumulative, preferably one, C—C double bonds in the ring. Examples for C₅-C₆-cycloalkenyl are cyclopent-1-en-1-yl, cyclopent-1-en-3-yl, cyclopent-1-en-4-yl, cyclopenta-1,3-dien-1-yl, cyclopenta-1,3-dien-2-yl, cyclopenta-1,3-dien-5-yl, cyclohex-1-en-1-yl, cyclohex-1-en-3-yl, cyclohex-1-en-4-yl, cyclohexa-1,3-dien-1-yl, cyclohexa-1,3-dien-2-yl, cyclohexa-1,3-dien-5-yl, cyclohexa-1,4-dien-1-yl and cyclohexa-1,4-dien-3-yl. Examples of C₅-C₇-cycloalkenyl are, apart those mentioned above, include for C₅-C₆-cycloalkenyl, cyclohept-1-en-1-yl, cyclohept-1-en-3-yl, cyclohept-1-en-4-yl, cyclohept-1-en-5-yl, cyclohepta-1,3-dien-1-yl, cyclohepta-1,3-dien-2-yl, cyclohepta-1,3-dien-5-yl, cyclohepta-1,3-dien-6-yl, cyclohepta-1,4-dien-1-yl, cyclohepta-1,4-dien-2-yl, cyclohepta-1,4-dien-3-yl and cyclohepta-1,4-dien-6-yl. Examples of C₃-C₈-cycloalkenyl are, apart those mentioned above for C₅-C₆-cycloalkenyl, cycloprop-1-en-1-yl, cycloprop-1-en-3-yl, cyclobut-1-en-1-yl, cyclobut-1-en-3-yl, cyclooct-1-en-1-yl, cyclooct-1-en-3-yl, cyclooct-1-en-4-yl, cyclooct-1-en-5-yl, cycloocta-1,3-dien-1-yl, cycloocta-1,3-dien-2-yl, cycloocta-1,3-dien-5-yl, cycloocta-1,3-dien-6-yl, cycloocta-1,4-dien-1-yl, cycloocta-1,4-dien-2-yl, cycloocta-1,4-dien-3-yl, cycloocta-1,4-dien-6-yl, cycloocta-1,4-dien-7-yl, cycloocta-1,5-dien-1-yl, and cycloocta-1,5-dien-3-yl.

The term “fluorinated cycloalkenyl” as used herein refers to monocyclic partially unsaturated, non-aromatic hydrocarbon radicals having 3 to 8 (“fluorinated C₃-C₈-cycloalkenyl”), in particular 5 to 7 carbon atoms (“fluorinated C₅-C₇-cycloalkenyl”) or 5 or 6 carbon atoms (“fluorinated C₅-C₆-cycloalkenyl”) and one or more non-cumulative, preferably one, C—C double bonds in the ring and in which some or all of the hydrogen atoms are replaced by fluorine atoms.

The term “cycloalkyl-C₁-C₄-alkyl” refers to a C₃-C₈-cycloalkyl group (“C₃-C₈-cycloalkyl-C₁-C₄-alkyl”), preferably a C₃-C₆-cycloalkyl group (“C₃-C₆-cycloalkyl-C₁-C₄-alkyl”) as defined above which is bound to the remainder of the molecule via a C₁-C₄-alkyl group, as defined above. The term “cycloalkyl-C₁-C₂-alkyl” refers to a C₃-C₈-cycloalkyl group (“C₃-C₈-cycloalkyl-C₁-C₂-alkyl”), preferably a C₃-C₆-cycloalkyl group (“C₃-C₆-cycloalkyl-C₁-C₂-alkyl”) as defined above which is bound to the remainder of the molecule via a C₁-C₂-alkyl group, as defined above. Examples for C₃-C₆-cycloalkyl-C₁-C₂-alkyl are cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopentylmethyl, cyclopentylethyl, cyclohexylmethyl and cyclohexylethyl. Examples for C₃-C₆-cycloalkyl-C₁-C₄-alkyl, apart those mentioned for C₃-C₆-cycloalkyl-C₁-C₂-alkyl, are cyclopropylpropyl, cyclopropylbutyl, cyclobutylpropyl, cyclobutylbutyl, cyclopentylpropyl, cyclopentylbutyl, cyclohexylpropyl and cyclohexylbutyl. Examples for C₃-C₈-cycloalkyl-C₁-C₂-alkyl, apart those mentioned for C₃-C₆-cycloalkyl-C₁-C₂-alkyl, are cycloheptylmethyl, cycloheptylethyl, cyclooctylmethyl and cyclooctylethyl. Examples for C₃-C₈-cycloalkyl-C₁-C₄-alkyl, apart those mentioned for C₃-C₈-cycloalkyl-C₁-C₂-alkyl, are cycloheptylpropyl, cycloheptylbutyl, cyclooctylpropyland cyclooctylbutyl.

The term “fluorinated cycloalkyl-C₁-C₄-alkyl” refers to a fluorinated C₃-C₈-cycloalkyl group (“fluorinated C₃-C₈-cycloalkyl-C₁-C₄-alkyl”), preferably a fluorinated C₃-C₆-cycloalkyl group (“fluorinated C₃-C₆-cycloalkyl-C₁-C₄-alkyl”) as defined above which is bound to the remainder of the molecule via a C₁-C₄-alkyl group, as defined above. The term “fluorinated cycloalkyl-C₁-C₂-alkyl” refers to a fluorinated C₃-C₈-cycloalkyl group (“fluorinated C₃-C₈-cycloalkyl-C₁-C₂-alkyl”), preferably a fluorinated C₃-C₆-cycloalkyl group (“fluorinated C₃-C₆-cycloalkyl-C₁-C₂-alkyl”) as defined above which is bound to the remainder of the molecule via a C₁-C₂-alkyl group, as defined above.

The term “C₁-C₂-alkoxy” is a C₁-C₂-alkyl group, as defined above, attached via an oxygen atom. The term “C₁-C₃-alkoxy” is a C₁-C₃-alkyl group, as defined above, attached via an oxygen atom. The term “C₁-C₄-alkoxy” is a C₁-C₄-alkyl group, as defined above, attached via an oxygen atom. The term “C₁-C₆-alkoxy” is a C₁-C₆-alkyl group, as defined above, attached via an oxygen atom. C₁-C₂-Alkoxy is methoxy or ethoxy. C₁-C₃-Alkoxy is additionally, for example, n-propoxy and 1-methylethoxy (isopropoxy). C₁-C₄-Alkoxy is additionally, for example, butoxy, 1-methylpropoxy (sec-butoxy), 2-methylpropoxy (isobutoxy) or 1,1-dimethylethoxy (tert-butoxy). C₁-C₆-Alkoxy is additionally, for example, pentoxy, 1-methylbutoxy, 2-methylbutoxy, 3-methylbutoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy, 1,2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy or 1-ethyl-2-methylpropoxy. C₁-C₈-Alkoxy is additionally, for example, heptyloxy, octyloxy, 2-ethylhexyloxy and positional isomers thereof.

The term “fluorinated C₁-C₂-alkoxy” is a fluorinated C₁-C₂-alkyl group, as defined above, attached via an oxygen atom. The term “fluorinated C₁-C₃-alkoxy” is a fluorinated C₁-C₃-alkyl group, as defined above, attached via an oxygen atom. The term “fluorinated C₁-C₆-haloalkoxy” is a fluorinated C₁-C₆-alkyl group, as defined above, attached via an oxygen atom. Fluorinated C₁-C₂-alkoxy is, for example, OCH₂F, OCHF₂, OCF₃, 1-fluoroethoxy, (R)-1-fluoroethoxy, (S)-1-fluoroethoxy, 2-fluoroethoxy, 1,1-difluoroethoxy, 1,2-difluoroethoxy, 2,2-difluoroethoxy, 1,1,2-trifluoroethoxy, 1,2,2-trifluoroethoxy, 2,2,2-trifluoroethoxy, 1,1,2,2-tetrafluoroethoxy or OC₂F₅. Fluorinated C₁-C₃-alkoxy is additionally, for example, 1-fluoropropoxy, (R)-1-fluoropropoxy, (S)-1-fluoropropoxy, 2-fluoropropoxy, (R)-2-fluoropropoxy, (S)-2-fluoropropoxy, 3-fluoropropoxy, 1,1-difluoropropoxy, 2,2-difluoropropoxy, 2,3-difluoropropoxy, 3,3-difluoropropoxy, 3,3,3-trifluoropropoxy, (R)-2-fluoro-1-methylethoxy, (S)-2-fluoro-1-methylethoxy, (R)-2,2-difluoro-1-methylethoxy, (S)-2,2-difluoro-1-methylethoxy, (R)-1,2-difluoro-1-methylethoxy, (S)-1,2-difluoro-1-methylethoxy, (R)-2,2,2-trifluoro-1-methylethoxy, (S)-2,2,2-trifluoro-1-methylethoxy, 2-fluoro-1-(fluoromethyl)ethoxy, 1-(difluoromethyl)-2,2-difluoroethoxy, OCH₂—C₂F₅, OCF₂—C₂F₅ or 1-(CH₂F)-2-fluoroethoxy. Fluorinated C₁-C₄-alkoxy is additionally, for example, 1-fluorobutoxy, (R)-1-fluorobutoxy, (S)-1-fluorobutoxy, 2-fluorobutoxy, 3-fluorobutoxy, 4-fluorobutoxy, 1,1-difluorobutoxy, 2,2-difluorobutoxy, 3,3-difluorobutoxy, 4,4-difluorobutoxy, 4,4,4-trifluorobutoxy or nonafluorobutoxy. Fluorinated C₁-C₆-alkoxy is additionally, for example, 5-fluoropentoxy, undecafluoropentoxy, 6-fluorohexoxy or tridecafluorohexoxy.

The term “C₁-C₄-alkoxy-C₁-C₄-alkyl” as used herein, refers to a straight-chain or branched alkyl group having 1 to 4 carbon atoms, as defined above, where one hydrogen atom is replaced by a C₁-C₄-alkoxy group, as defined above. The term “C₁-C₆-alkoxy-C₁-C₄-alkyl” as used herein, refers to a straight-chain or branched alkyl group having 1 to 4 carbon atoms, as defined above, where one hydrogen atom is replaced by a C₁-C₆-alkoxy group, as defined above. Examples are methoxymethyl, ethoxymethyl, propoxymethyl, isopropoxymethyl, n-butoxymethyl, sec-butoxymethyl, isobutoxymethyl, tert-butoxymethyl, 1-methoxyethyl, 1-ethoxyethyl, 1-propoxyethyl, 1-isopropoxyethyl, 1-n-butoxyethyl, 1-sec-butoxyethyl, 1-isobutoxyethyl, 1-tert-butoxyethyl, 2-methoxyethyl, 2-ethoxyethyl, 2-propoxyethyl, 2-isopropoxyethyl, 2-n-butoxyethyl, 2-sec-butoxyethyl, 2-isobutoxyethyl, 2-tert-butoxyethyl, 1-methoxypropyl, 1-ethoxypropyl, 1-propoxypropyl, 1-isopropoxypropyl, 1-n-butoxypropyl, 1-sec-butoxypropyl, 1-isobutoxypropyl, 1-tert-butoxypropyl, 2-methoxypropyl, 2-ethoxypropyl, 2-propoxypropyl, 2-isopropoxypropyl, 2-n-butoxypropyl, 2-sec-butoxypropyl, 2-isobutoxypropyl, 2-tert-butoxypropyl, 3-methoxypropyl, 3-ethoxypropyl, 3-propoxypropyl, 3-isopropoxypropyl, 3-n-butoxypropyl, 3-sec-butoxypropyl, 3-isobutoxypropyl, 3-tert-butoxypropyl and the like.

The term “hydroxy-C₁-C₄-alkyl” as used herein, refers to a straight-chain or branched alkyl group having 1 to 4 carbon atoms, as defined above, where one hydrogen atom is replaced by a hydroxy group. The term “hydroxy-C₁-C₆-alkyl” as used herein, refers to a straight-chain or branched alkyl group having 1 to 6 carbon atoms, as defined above, where one hydrogen atom is replaced by a hydroxy group. Examples for hydroxy-C₁-C₄-alkyl include hydroxymethyl, 1-hydroxyethyl, 2-hydroxyethyl, 1-hydroxypropyl, 2-hydroxypropyl, 3-hydroxypropyl, 1-hydroxyprop-2-yl, 2-hydroxyprop-2-yl, 1-hydroxybutyl, 2-hydroxybutyl, 3-hydroxybutyl, 4-hydroxybutyl, 1-hydroxybut-2-yl, 2-hydroxybut-2-yl, 3-hydroxybut-2-yl, 4-hydroxybut-2-yl, hydroxy-tert-butyl and the like. Examples for hydroxy-C₁-C₆-alkyl are, apart those mentioned for hydroxy-C₁-C₄-alkyl, include, 1-hydroxypentyl, 2-hydroxypentyl, 3-hydroxypentyl, 4-hydroxypentyl, 5-hydroxypentyl, 1-hydroxyhexyl, 2-hydroxyhexyl, 3-hydroxyhexyl, 4-hydroxyhexyl, 5-hydroxyhexyl, 6-hydroxyhexyl and the like.

The term “hydroxy-C₁-C₄-alkoxy” as used herein, refers to a C₁-C₄-alkoxy group, as defined above, where one hydrogen atom is replaced by a hydroxy group. The term “hydroxy-C₁-C₆-alkoxy” as used herein, refers to a C₁-C₆-alkoxy group, as defined above, where one hydrogen atom is replaced by a hydroxy group. Examples for hydroxy-C₁-C₄-alkoxy include hydroxymethoxy, 1-hydroxyethoxy, 2-hydroxyethoxy, 1-hydroxypropoxy, 2-hydroxypropoxy, 3-hydroxypropoxy, 1-hydroxy-2-propoxy, 2-hydroxy-2-propoxy, 1-hydroxybutoxy, 2-hydroxybutoxy, 3-hydroxybutoxy, 4-hydroxybutoxy, 1-hydroxy-2-butoxy, 2-hydroxy-2-butoxy, 3-hydroxy-2-butoxy, 4-hydroxy-2-butoxy, hydroxy-tert-butoxy and the like. Examples for hydroxy-C₁-C₆-alkoxy include, apart those mentioned for hydroxy-C₁-C₄-alkoxy, 1-hydroxypentoxy, 2-hydroxypentoxy, 3-hydroxypentoxy, 4-hydroxypentoxy, 5-hydroxypentoxy, 1-hydroxyhexoxy, 2-hydroxyhexoxy, 3-hydroxyhexoxy, 4-hydroxyhexoxy, 5-hydroxyhexoxy, 6-hydroxyhexoxy and the like.

The term “C₁-C₄-alkoxy-C₁-C₄-alkoxy” as used herein, refers to a C₁-C₄-alkoxy group, as defined above, where one hydrogen atom is replaced by a C₁-C₄-alkoxy group, as defined above. The term “C₁-C₆-alkoxy-C₁-C₄-alkoxy” as used herein, refers to a C₁-C₄-alkoxy group, as defined above, where one hydrogen atom is replaced by a C₁-C₄-alkoxy group, as defined above. Examples are methoxymethoxy, ethoxymethoxy, propoxymethoxy, isopropoxymethoxy, butoxymethoxy, sec-butoxymethoxy, isobutoxymethoxy, tert-butoxymethoxy, 1-methoxyethoxy, 1-ethoxyethoxy, 1-propoxyethoxy, 1-isopropoxyethoxy, 1-butoxyethoxy, 1-sec-butoxyethoxy, 1-isobutoxyethoxy, 1-tert-butoxyethoxy, 2-methoxyethoxy, 2-ethoxyethoxy, 2-propoxyethoxy, 2-isopropoxyethoxy, 2-butoxyethoxy, 2-sec-butoxyethoxy, 2-isobutoxyethoxy, 2-tert-butoxyethoxy, 1-methoxypropoxy, 1-ethoxypropoxy, 1-propoxypropoxy, 1-isopropoxypropoxy, 1-butoxypropoxy, 1-sec-butoxypropoxy, 1-isobutoxypropoxy, 1-tert-butoxypropoxy, 2-methoxypropoxy, 2-ethoxypropoxy, 2-propoxypropoxy, 2-isopropoxypropoxy, 2-butoxypropoxy, 2-sec-butoxypropoxy, 2-isobutoxypropoxy, 2-tert-butoxypropoxy, 3-methoxypropoxy, 3-ethoxypropoxy, 3-propoxypropoxy, 3-isopropoxypropoxy, 3-butoxypropoxy, 3-sec-butoxypropoxy, 3-isobutoxypropoxy, 3-tert-butoxypropoxy and the like.

The term “C₁-C₂-alkylthio” is a C₁-C₂-alkyl group, as defined above, attached via a sulfur atom. The term “C₁-C₃-alkylthio” refers to a C₁-C₃-alkyl group, as defined above, attached via a sulfur atom. The term “C₁-C₄-alkylthio” is a C₁-C₄-alkyl group, as defined above, attached via a sulfur atom. The term “C₁-C₆-alkylthio” refers to a C₁-C₆-alkyl group, as defined above, attached via a sulfur atom. The term “C₁-C₁₀-alkylthio” refers to a C₁-C₁₀-alkyl group, as defined above, attached via a sulfur atom. C₁-C₂-Alkylthio is methylthio or ethylthio. C₁-C₃-Alkylthio is additionally, for example, n-propylthio or 1-methylethylthio (isopropylthio). C₁-C₄-Alkylthio is additionally, for example, butylthio, 1-methylpropylthio (sec-butylthio), 2-methylpropylthio (isobutylthio) or 1,1-dimethylethylthio (tert-butylthio). C₁-C₆-Alkylthio is additionally, for example, pentylthio, 1-methylbutylthio, 2-methylbutylthio, 3-methylbutylthio, 1,1-dimethylpropylthio, 1,2-dimethylpropylthio, 2,2-dimethylpropylthio, 1-ethylpropylthio, hexylthio, 1-methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio, 1,1-dimethylbutylthio, 1,2-dimethylbutylthio, 1,3-dimethylbutylthio, 2,2-dimethylbutylthio, 2,3-dimethylbutylthio, 3,3-dimethylbutylthio, 1-ethylbutylthio, 2-ethylbutylthio, 1,1,2-trimethylpropylthio, 1,2,2-trimethylpropylthio, 1-ethyl-1-methylpropylthio or 1-ethyl-2-methylpropylthio.

The term “fluorinated C₁-C₂-alkylthio” refers to a fluorinated C₁-C₂-alkyl group, as defined above, attached via a sulfur atom. The term “fluorinated C₁-C₃-alkylthio” refers to a fluorinated C₁-C₃-alkyl group, as defined above, attached via a sulfur atom. The term “fluorinated C₁-C₄-alkylthio” refers to a fluorinated C₁-C₄-alkyl group, as defined above, attached via a sulfur atom. The term “fluorinated C₁-C₆-alkylthio” refers to a fluorinated C₁-C₆-alkyl group, as defined above, attached via a sulfur atom. Fluorinated C₁-C₂-alkylthio refers to, for example, SCH₂F, SCHF₂, SCF₃, 2-fluoroethylthio, 2,2-difluoroethylthio, 2,2,2-trifluoroethylthio, or SC₂F₅. Fluorinated C₁-C₃-alkylthio may additionally, for example, include 2-fluoropropylthio, 3-fluoropropylthio, 2,2-difluoropropylthio, 2,3-difluoropropylthio, 3,3,3-trifluoropropylthio, SCH₂—C₂F₅, SCF₂—C₂F₅ or 1-(CH₂F)-2-fluoroethylthio. Fluorinated C₁-C₄-alkylthio may additionally, for example, include 4-fluorobutylthio or nonafluorobutylthio. Fluorinated C₁-C₆-alkylthio is additionally, for example, 5-fluoropentylthio, undecafluoropentylthio, 6-fluorohexylthio or dodecafluorohexylthio.

The term “C₁-C₂-alkylsulfinyl” refers to a C₁-C₂-alkyl group, as defined above, attached via a sulfinyl [S(O)] group. The term “C₁-C₄-alkylsulfinyl” is a C₁-C₄-alkyl group, as defined above, attached via a sulfinyl [S(O)] group. The term “C₁-C₆-alkylsulfinyl” is a C₁-C₆-alkyl group, as defined above, attached via a sulfinyl [S(O)] group. C₁-C₂-Alkylsulfinyl is methylsulfinyl or ethylsulfinyl. C₁-C₄-Alkylsulfinyl is additionally, for example, n-propylsulfinyl, 1-methylethylsulfinyl (isopropylsulfinyl), butylsulfinyl, 1-methylpropylsulfinyl (sec-butylsulfinyl), 2-methylpropylsulfinyl (isobutylsulfinyl) or 1,1-dimethylethylsulfinyl (tert-butylsulfinyl). C₁-C₆-Alkylsulfinyl is additionally, for example, pentylsulfinyl, 1-methylbutylsulfinyl, 2-methylbutylsulfinyl, 3-methylbutylsulfinyl, 1,1-dimethylpropylsulfinyl, 1,2-dimethylpropylsulfinyl, 2,2-dimethylpropylsulfinyl, 1-ethylpropylsulfinyl, hexylsulfinyl, 1-methylpentylsulfinyl, 2-methylpentylsulfinyl, 3-methylpentylsulfinyl, 4-methylpentylsulfinyl, 1,1-dimethylbutylsulfinyl, 1,2-dimethylbutylsulfinyl, 1,3-dimethylbutylsulfinyl, 2,2-dimethylbutylsulfinyl, 2,3-dimethylbutylsulfinyl, 3,3-dimethylbutylsulfinyl, 1-ethylbutylsulfinyl, 2-ethylbutylsulfinyl, 1,1,2-trimethylpropylsulfinyl, 1,2,2-trimethylpropylsulfinyl, 1-ethyl-1-methylpropylsulfinyl or 1-ethyl-2-methylpropylsulfinyl.

The term “fluorinated C₁-C₂-alkylsulfinyl” refers to a fluorinated C₁-C₂-alkyl group, as defined above, attached via a sulfinyl [S(O)] group. The term “fluorinated C₁-C₃-alkylsulfinyl” refers to a fluorinated C₁-C₃-alkyl group, as defined above, attached via a sulfinyl [S(O)] group. The term “fluorinated C₁-C₄-alkylsulfinyl” refers to a fluorinated C₁-C₄-alkyl group, as defined above, attached via a sulfinyl [S(O)] group. The term “fluorinated C₁-C₆-alkylsulfinyl” refers to a fluorinated C₁-C₆-alkyl group, as defined above, attached via a sulfinyl [S(O)] group. Fluorinated C₁-C₂-alkylsulfinyl is, for example, S(O)CH₂F, S(O)CHF₂, S(O)CF₃, 2-fluoroethylsulfinyl, 2,2-difluoroethylsulfinyl, 2,2,2-trifluoroethylsulfinyl, or S(O)C₂F₅. Fluorinated C₁-C₃-alkylsulfinyl may additionally, for example, include 2-fluoropropylsulfinyl, 3-fluoropropylsulfinyl, 2,2-difluoropropylsulfinyl, 2,3-difluoropropylsulfinyl, 3,3,3-trifluoropropylsulfinyl, S(O)CH₂—C₂F₅, S(O)CF₂—C₂F₅ or 1-(CH₂F)-2-fluoroethylsulfinyl. Fluorinated C₁-C₄-alkylsulfinyl may additionally, for example, include 4-fluorobutylsulfinyl or nonafluorobutylsulfinyl. Fluorinated C₁-C₆-alkylsulfinyl may additionally, for example, include 5-fluoropentylsulfinyl, undecafluoropentylsulfinyl, 6-fluorohexylsulfinyl or dodecafluorohexylsulfinyl.

The term “C₁-C₂-alkylsulfonyl” refers to a C₁-C₂-alkyl group, as defined above, attached via a sulfonyl [S(O)₂] group. The term “C₁-C₄-alkylsulfonyl” refers to a C₁-C₄-alkyl group, as defined above, attached via a sulfonyl [S(O)₂] group. The term “C₁-C₆-alkylsulfonyl” is a C₁-C₆-alkyl group, as defined above, attached via a sulfonyl [S(O)₂] group. C₁-C₂-Alkylsulfonyl refers to a methylsulfonyl or ethylsulfonyl. C₁-C₄-Alkylsulfonyl is additionally, for example, n-propylsulfonyl, 1-methylethylsulfonyl (isopropylsulfonyl), butylsulfonyl, 1-methylpropylsulfonyl (sec-butylsulfonyl), 2-methylpropylsulfonyl (isobutylsulfonyl) or 1,1-dimethylethylsulfonyl (tert-butylsulfonyl). C₁-C₆-Alkylsulfonyl is additionally, for example, pentylsulfonyl, 1-methylbutylsulfonyl, 2-methylbutylsulfonyl, 3-methylbutylsulfonyl, 1,1-dimethylpropylsulfonyl, 1,2-dimethylpropylsulfonyl, 2,2-dimethylpropylsulfonyl, 1-ethylpropylsulfonyl, hexylsulfonyl, 1-methylpentylsulfonyl, 2-methylpentylsulfonyl, 3-methylpentylsulfonyl, 4-methylpentylsulfonyl, 1,1-dimethylbutylsulfonyl, 1,2-dimethylbutylsulfonyl, 1,3-dimethylbutylsulfonyl, 2,2-dimethylbutylsulfonyl, 2,3-dimethylbutylsulfonyl, 3,3-dimethylbutylsulfonyl, 1-ethylbutylsulfonyl, 2-ethylbutylsulfonyl, 1,1,2-trimethylpropylsulfonyl, 1,2,2-trimethylpropylsulfonyl, 1-ethyl-1-methylpropylsulfonyl or 1-ethyl-2-methylpropylsulfonyl.

The term “fluorinated C₁-C₂-alkylsulfonyl” refers to a fluorinated C₁-C₂-alkyl group, as defined above, attached via a sulfonyl [S(O)₂] group. The term “fluorinated C₁-C₃-alkylsulfonyl” refers to a fluorinated C₁-C₃-alkyl group, as defined above, attached via a sulfonyl [S(O)₂] group. The term “fluorinated C₁-C₄-alkylsulfonyl” refers to a fluorinated C₁-C₄-alkyl group, as defined above, attached via a sulfonyl [S(O)₂] group. The term “fluorinated C₁-C₆-alkylsulfonyl” refers to a fluorinated C₁-C₆-alkyl group, as defined above, attached via a sulfonyl [S(O)₂] group. Fluorinated C₁-C₂-alkylsulfonyl is, for example, S(O)₂CH₂F, S(O)₂CHF₂, S(O)₂CF₃, 2-fluoroethylsulfonyl, 2,2-difluoroethylsulfonyl, 2,2,2-trifluoroethylsulfonyl, or S(O)₂C₂F₅. Fluorinated C₁-C₃-alkylsulfonyl is additionally, for example, 2-fluoropropylsulfonyl, 3-fluoropropylsulfonyl, 2,2-difluoropropylsulfonyl, 2,3-difluoropropylsulfonyl, 3,3,3-trifluoropropylsulfonyl, S(O)₂CH₂—C₂F5, S(O)₂CF₂—C₂F₅ or 1-(CH₂F)-2-fluoroethylsulfonyl. Fluorinated C₁-C₄-alkylsulfonyl is additionally, for example, 4-fluorobutylsulfonyl or nonafluorobutylsulfonyl. Fluorinated C₁-C₆-alkylsulfonyl is additionally, for example, 5-fluoropentylsulfonyl, undecafluoropentylsulfonyl, 6-fluorohexylsulfonyl or dodecafluorohexylsulfonyl.

C₁-C₄-Alkylcarbonyl refers to a straight-chain or branched alkyl group having from 1 to 4 carbon atoms), which is bound to the remainder of the molecule via a carbonyl group (CO), such as in acetyl, propionyl, isopropylcarbonyl, butylcarbonyl, sec-butylcarbonyl, isobutylcarbonyl, and tert-butylcarbonyl. C₁-C₆-Alkylcarbonyl is a straight-chain or branched alkyl group having from 1 to 6 carbon atoms, which is bound to the remainder of the molecule via a carbonyl group (CO). Examples include, apart those listed above for C₁-C₄-alkylcarbonylpentylcarbonyl, hexylcarbonyl and the constitutional isomers thereof.

Fluorinated C₁-C₄-alkylcarbonyl refers to a straight-chain or branched fluorinated alkyl group having from 1 to 4 carbon atoms as defined above, which is bound to the remainder of the molecule via a carbonyl group (CO). Fluorinated C₁-C₆-alkylcarbonyl is a straight-chain or branched fluorinated alkyl group having from 1 to 6 carbon atoms as defined above, which is bound to the remainder of the molecule via a carbonyl group (CO). Examples include trifluoromethylcarbonyl, 2,2,2-trifluoroethylcarbonyl and the like.

C₃-C₆-cycloalkylcarbonyl relates to a C₃-C₆-cycloalkyl group as defined above which is bound to the remainder of the molecule via a carbonyl group (CO), such as in cyclopropylcarbonyl, cyclobutylcarbonyl, cyclopentylcarbonyl and cyclohexylcarbonyl.

C₁-C₆-Alkoxycarbonyl refers to a straight-chain or branched alkoxy group having from 1 to 6, especially 1 to 4 carbon atoms (═C₁-C₄-alkoxycarbonyl), in particular 1 to 3 carbon atoms (═C₁-C₃-alkoxycarbonyl), which is bound to the remainder of the molecule via a carbonyl group (CO), such as in methoxycarbonyl, ethoxycarbonyl, propyloxycarbonyl, and isopropyloxycarbonyl.

Fluorinated C₁-C₆-alkoxycarbonyl refers to a straight-chain or branched fluorinated alkoxy group having from 1 to 6, especially 1 to 4 carbon atoms (=fluorinated C₁-C₄-alkoxycarbonyl), in particular 1 to 3 carbon atoms (=fluorinated C₁-C₃-alkoxycarbonyl) as defined above, which is bound to the remainder of the molecule via a carbonyl group (CO). Examples include trifluoromethoxycarbonyl, 2,2,2-trifluoroethoxycarbonyl and the like.

C₁-C₄-Alkylcarbonyloxy refers to a straight-chain or branched alkyl group having from 1 to 4 carbon atoms, which is bound to the remainder of the molecule via a carbonyloxy group [C(O)—O—], such as in acet(yl)oxy, propionyloxy, isopropylcarbonyloxy, butylcarbonyloxy, sec-butylcarbonyloxy, isobutylcarbonyloxy, and tert-butylcarbonyloxy. C₁-C₆-Alkylcarbonyloxy is a straight-chain or branched alkyl group having from 1 to 6 carbon atoms, which is bound to the remainder of the molecule via a carbonyloxy group [C(O—O—]. Examples include, apart those listed above for C₁-C₄-alkylcarbonyloxy, pentylcarbonyloxy, hexylcarbonyloxy and the constitutional isomers thereof.

Fluorinated C₁-C₄-alkylcarbonyloxy refers to a straight-chain or branched fluorinated alkyl group having from 1 to 4 carbon atoms as defined above, which is bound to the remainder of the molecule via a carbonyloxy group [C(O)—O—]. Fluorinated C₁-C₆-alkylcarbonyloxy is a straight-chain or branched fluorinated alkyl group having from 1 to 6 carbon atoms as defined above, which is bound to the remainder of the molecule via a carbonyloxy group [C(O)—O—]. Examples include trifluoromethylcarbonyloxy, 2,2,2-trifluoroethylcarbonyloxy and the like.

Phenyl-C₁-C₂-alkyl is a phenyl group bound to the remainder of the molecule via a C₁-C₂-alkyl group. Examples are benzyl, 1-phenylethyl and 2-phenylethyl (phenethyl).

The term “3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated heterocyclic ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups as ring members” denotes a 3-, 4-, 5-, 6-, 7- or 8-membered, preferably a 3-, 4-, 5-, 6- or 7-membered saturated, partially unsaturated or maximum unsaturated heteromonocyclic ring containing 1, 2, 3 or 4 (preferably 1, 2 or 3) heteroatoms or heteroatom groups selected from N, O, S, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups as ring members.

Unsaturated rings contain at least one C—C and/or C—N and/or N—N double bond(s). Maximally unsaturated rings contain as many conjugated C—C and/or C—N and/or N—N double bonds as allowed by the ring size. Maximally unsaturated 5- or 6-membered heterocyclic rings are aromatic. 7- and 8-membered rings cannot be aromatic. They are homoaromatic (7-membered ring, 3 double bonds) or have 4 double bonds (8-membered ring). Partially unsaturated rings contain less than the maximum number of C—C and/or C—N and/or N—N double bond(s) allowed by the ring size. The heterocyclic ring may be attached to the remainder of the molecule via a carbon ring member or via a nitrogen ring member. As a matter of course, the heterocyclic ring contains at least one carbon ring atom. If the ring contains more than one O ring atom, these are not adjacent.

Examples of a 3-, 4-, 5-, 6- or 7-membered saturated heterocyclic ring include: Oxiranyl, thiiranyl, aziridinyl, oxetanyl, thietanyl, azetidinyl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, tetrahydrofuran-2-on-3-yl, tetrahydrofuran-2-on-4-yl, tetrahydrofuran-2-on-5-yl, tetrahydrofuran-2-thion-3-yl, tetrahydrofuran-2-thion-4-yl, tetrahydrofuran-2-thion-5-yl, tetrahydrothien-2-yl, tetrahydrothien-3-yl, tetrahydrothien-2-on-3-yl, tetrahydrothien-2-on-4-yl, tetrahydrothien-2-on-5-yl, tetrahydrothien-2-thion-3-yl, tetrahydrothien-2-thion-4-yl, tetrahydrothien-2-thion-5-yl, pyrrolidin-1-yl, pyrrolidine-2-on-1-yl, pyrrolidine-2,5-dion-1-yl, pyrrolidine-2-thion-1-yl, pyrrolidin-2-yl, pyrrolidin-3-yl, pyrrolidine-2-on-3-yl, pyrrolidine-2-on-4-yl, pyrrolidine-2-on-5-yl, pyrrolidine-2,5-dion-3-yl, pyrrolidine-2-thion-3-yl, pyrrolidine-2-thion-4-yl, pyrrolidine-2-thion-5-yl, pyrazolidin-1-yl, pyrazolidin-3-yl, pyrazolidin-4-yl, pyrazolidin-5-yl, imidazolidin-1-yl, imidazolidin-2-on-1-yl, imidazolidin-2-thion-1-yl, imidazolidin-2-yl, imidazolidin-4-yl, imidazolidin-2-on-4-yl, imidazolidin-2-thion-4-yl, oxazolidin-2-yl, oxazolidin-3-yl, oxazolidin-4-yl, oxazolidin-5-yl, isoxazolidin-2-yl, isoxazolidin-3-yl, isoxazolidin-4-yl, isoxazolidin-5-yl, thiazolidin-2-yl, thiazolidin-3-yl, thiazolidin-4-yl, thiazolidin-5-yl, isothiazolidin-2-yl, isothiazolidin-3-yl, isothiazolidin-4-yl, isothiazolidin-5-yl, 1,2,4-oxadiazolidin-3-yl, 1,2,4-oxadiazolidin-5-yl, 1,2,4-thiadiazolidin-3-yl, 1,2,4-thiadiazolidin-5-yl, 1,2,4-triazolidin-3-yl, 1,3,4-oxadiazolidin-2-yl, 1,3,4-thiadiazolidin-2-yl, 1,3,4-triazolidin-1-yl, 1,3,4-triazolidin-2-yl, 2-tetrahydropyranyl, 4-tetrahydropyranyl, 1,3-dioxan-5-yl, 1,4-dioxan-2-yl, piperidin-1-yl, piperidin-2-on-1-yl, piperidin-2,5-dion-1-yl, piperidine-2-thion-1-yl, piperidin-2-yl, piperidin-3-yl, piperidin-2-on-3-yl, piperidin-2,5-dion-3-yl, piperidin-2-thion-3-yl, piperidin-4-yl, hexahydropyridazin-3-yl, hexahydropyridazin-4-yl, hexahydropyrimidin-2-yl, hexahydropyrimidin-4-yl, hexahydropyrimidin-5-yl, piperazin-1-yl, piperazin-2-yl, 1,3,5-hexahydrotriazin-1-yl, 1,3,5-hexahydrotriazin-2-yl and 1,2,4-hexahydrotriazin-3-yl, morpholin-2-yl, morpholin-3-yl, morpholin-4-yl, thiomorpholin-2-yl, thiomorpholin-3-yl, thiomorpholin-4-yl, 1-oxothiomorpholin-2-yl, 1-oxothiomorpholin-3-yl, 1-oxothiomorpholin-4-yl, 1,1-dioxothiomorpholin-2-yl, 1,1-dioxothiomorpholin-3-yl, 1,1-dioxothiomorpholin-4-yl, azepan-1-, -2-, -3- or -4-yl, oxepan-2-, -3-, -4- or -5-yl, hexahydro-1,3-diazepinyl, hexahydro-1,4-diazepinyl, hexahydro-1,3-oxazepinyl, hexahydro-1,4-oxazepinyl, hexahydro-1,3-dioxepinyl, hexahydro-1,4-dioxepinyl and the like.

Examples of a 3-, 4-, 5-, 6-, 7- or 8-membered saturated heterocyclic ring further include oxocane, thiocane, azocane, [1,3]diazocane, [1,4]diazocane, [1,5]diazocane, [1,5]oxazocane and the like.

Examples of a 3-, 4-, 5-, 6- or 7-membered partially unsaturated heterocyclic ring include: 2,3-dihydrofur-2-yl, 2,3-dihydrofur-3-yl, 2,4-dihydrofur-2-yl, 2,4-dihydrofur-3-yl, 2,3-dihydrothien-2-yl, 2,3-dihydrothien-3-yl, 2,4-dihydrothien-2-yl, 2,4-dihydrothien-3-yl, 2-pyrrolin-2-yl, 2-pyrrolin-3-yl, 3-pyrrolin-2-yl, 3-pyrrolin-3-yl, 2-isoxazolin-3-yl, 3-isoxazolin-3-yl, 4-isoxazolin-3-yl, 2-isoxazolin-4-yl, 3-isoxazolin-4-yl, 4-isoxazolin-4-yl, 2-isoxazolin-5-yl, 3-isoxazolin-5-yl, 4-isoxazolin-5-yl, 2-isothiazolin-3-yl, 3-isothiazolin-3-yl, 4-isothiazolin-3-yl, 2-isothiazolin-4-yl, 3-isothiazolin-4-yl, 4-isothiazolin-4-yl, 2-isothiazolin-5-yl, 3-isothiazolin-5-yl, 4-isothiazolin-5-yl, 2,3-dihydropyrazol-1-yl, 2,3-dihydropyrazol-2-yl, 2,3-dihydropyrazol-3-yl, 2,3-dihydropyrazol-4-yl, 2,3-dihydropyrazol-5-yl, 3,4-dihydropyrazol-1-yl, 3,4-dihydropyrazol-3-yl, 3,4-dihydropyrazol-4-yl, 3,4-dihydropyrazol-5-yl, 4,5-dihydropyrazol-1-yl, 4,5-dihydropyrazol-3-yl, 4,5-dihydropyrazol-4-yl, 4,5-dihydropyrazol-5-yl, 2,3-dihydrooxazol-2-yl, 2,3-dihydrooxazol-3-yl, 2,3-dihydrooxazol-4-yl, 2,3-dihydrooxazol-5-yl, 3,4-dihydrooxazol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl, 3,4-dihydrooxazol-5-yl, 3,4-dihydrooxazol-2-yl, 3,4-dihydrooxazol-3-yl, 3,4-dihydrooxazol-4-yl, 2-, 3-, 4-, 5- or 6-di- or tetrahydropyridinyl, 3-di- or tetrahydropyridazinyl, 4-di- or tetrahydropyridazinyl, 2-di- or tetrahydropyrimidinyl, 4-di- or tetrahydropyrimidinyl, 5-di- or tetrahydropyrimidinyl, di- or tetrahydropyrazinyl, 1,3,5-di- or tetrahydrotriazin-2-yl, 1,2,4-di- or tetrahydrotriazin-3-yl, 2,3,4,5-tetrahydro[1H]azepin-1-, -2-, -3-, -4-, -5-, -6- or -7-yl, 3,4,5,6-tetrahydro[2H]azepin-2-, -3-, -4-, -5-, -6- or -7-yl, 2,3,4,7-tetrahydro[1H]azepin-1-, -2-, -3-, -4-, -5-, -6- or -7-yl, 2,3,6,7-tetrahydro[1H]azepin-1-, -2-, -3-, -4-, -5-, -6- or -7-yl, tetrahydrooxepinyl, such as 2,3,4,5-tetrahydro[1H]oxepin-2-, -3-, -4-, -5-, -6- or -7-yl, 2,3,4,7-tetrahydro[1H]oxepin-2-, -3-, -4-, -5-, -6- or -7-yl, 2,3,6,7-tetrahydro[1H]oxepin-2-, -3-, -4-, -5-, -6- or -7-yl, tetrahydro-1,3-diazepinyl, tetrahydro-1,4-diazepinyl, tetrahydro-1,3-oxazepinyl, tetrahydro-1,4-oxazepinyl, tetrahydro-1,3-dioxepinyl and tetrahydro-1,4-dioxepinyl.

Examples of a 3-, 4-, 5-, 6-, 7- or 8-membered partially unsaturated heterocyclic ring further include 1,2,3,4,5,6-hexahydroazocine, 2,3,4,5,6,7-hexahydroazocine, 1,2,3,4,5,8-hexahydroazocine, 1,2,3,4,7,8-hexahydroazocine, 1,2,3,4,5,6-hexahydro-[1,5]diazocine,1,2,3,4,7,8-hexahydro-[1,5]diazocine and the like.

Examples of a 3-, 4-, 5-, 6- or 7-membered maximally unsaturated (including aromatic) heterocyclic ring include 5- or 6-membered heteroaromatic rings, such as 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 1-pyrazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 1-imidazolyl, 2-imidazolyl, 4-imidazolyl, 1,3,4-triazol-1-yl, 1,3,4-triazol-2-yl, 2-pyridinyl, 3-pyridinyl, 4-pyridinyl, 1-oxopyridin-2-yl, 1-oxopyridin-3-yl, 1-oxopyridin-4-yl, 3-pyridazinyl, 4-pyridazinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl and 2-pyrazinyl, and also homoaromatic radicals, such as 1H-azepine, 1H-[1,3]-diazepine and 1H-[1,4]-diazepine.

Examples of a 3-, 4-, 5-, 6-, 7- or 8-membered maximally unsaturated heterocyclic ring further include [1,3]diazocine, [1,5]diazocine and [1,5]diazocine.

A 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members is either saturated, partially unsaturated and carbocyclic (if it contains only C═O and/or C═S as heteroatom group and no further heteroatoms or heteroatom groups) or saturated, partially unsaturated or maximally unsaturated heterocyclic. Examples are, in addition to the heterocyclic rings mentioned above, carbocyclic rings, such as cyclopropanonyl, cyclobutanonyl, cyclopentanonyl, cyclohexanonyl, cyclohexandionyl, cycloheptanonyl, cyclooctanonyl, cyclopropanthionyl, cyclobutanthionyl, cyclopentanthionyl, cyclohexanthionyl, cyclohexandithionyl, cycloheptanthionyl, cyclooctanthionyl, cyclopropenonyl, cyclopentenonyl, cyclohexenonyl and the like.

The remarks made above and in the following with respect to preferred aspects of the invention, e.g. to preferred meanings of the variables R¹, R², R^(3a), R^(3b), R^(4a), R^(4b), R^(5a), R^(5b), R⁶, R⁷, R⁸, R⁹, a, b and n of compounds I, to preferred compounds I and to preferred embodiments of the method or the use according to the invention, apply in each case on their own or in particular to combinations thereof.

In a preferred embodiment, R¹ is selected from hydrogen, cyano, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, —C(═O)R¹⁰, phenyl and benzyl, where the phenyl moiety in the two last-mentioned radicals may carry 1, 2 or 3 radicals R¹¹, where R¹⁰ and R¹¹ have one of the general meanings given above, or, in particular, one of the preferred meanings given below.

In the above group —C(═O)R¹⁰ as a meaning for R¹, R¹⁰ is preferably selected from C₁-C₄-alkyl and C₁-C₄-alkoxy and more preferably from C₁-C₂-alkyl and tert-butoxy.

More preferably, R¹ is selected from hydrogen and C₁-C₆-alkyl, in particular from hydrogen and methyl, and is specifically hydrogen.

In a preferred embodiment, R² is selected from cyano, nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy, more preferably from C₁-C₆-alkyl, in particular from methyl, ethyl, propyl and isopropyl, more particularly from methyl and ethyl, and is specifically methyl.

In a preferred embodiment, R^(3a) and R^(3b), independently of each other, are selected from hydrogen, cyano, nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy. More preferably, R^(3a) is selected from hydrogen, cyano, nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy, and R^(3b) is hydrogen. Even more preferably, R^(3a) is selected from hydrogen and methyl and R^(3b) is hydrogen. In particular, both R^(3a) and R^(3b) are hydrogen.

In a preferred embodiment, R^(4a) and R^(4b), independently of each other, are selected from hydrogen, C₁-C₆-alkyl and fluorinated C₁-C₆-alkyl or form together a group ═O.

More preferably, they are hydrogen or form together a group ═O. In another embodiment, one of R^(4a) and R^(4b) is hydrogen and the other is methyl; especially if X is CR⁷R⁸. In particular, both R^(4a) and R^(4b) are hydrogen.

In a preferred embodiment,

-   R^(5a) is selected from hydrogen, cyano, nitro, hydroxy,     C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated     C₁-C₆-alkoxy; and in case that X is CR⁷R⁸ is further selected from     halogen; or -   R^(5a) and R⁶, together with the atoms they are bound to, form a 3-,     4-, 5-, 6- or 7-membered saturated, partially unsaturated or     maximally unsaturated heterocyclic ring, where the ring may further     contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups     selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and     where the ring may be substituted with one or more substituents R¹¹;     or -   R^(5a) and R⁷, together with the carbon atoms they are bound to,     form a 3-, 4-, 5-, 6- or 7-membered saturated, partially unsaturated     or maximally unsaturated ring, where the ring may contain 1, 2, 3 or     4 heteroatoms or heteroatom-containing groups selected from O, S, N,     SO, SO₂, C═O and C═S as ring members, and where the ring may be     substituted with one or more substituents R¹¹; and -   R^(5b) is selected from hydrogen and deuterium and is preferably     hydrogen; where R¹¹ has one of the general meanings given above, or,     in particular, one of the preferred meanings given below.

More preferably,

-   R^(5a) is selected from hydrogen, C₁-C₆-alkyl and fluorinated     C₁-C₆-alkyl; and in case that     -   X is CR⁷R⁸ is further selected from halogen; and is preferably         selected from hydrogen and methyl, or     -   R^(5a) and R⁶ form together a group (CH₂)_(r), where r is 2, 3,         4 or 5, preferably 2, 3 or 4; or     -   R^(5a) and R⁷ form together a group (CH₂)_(s), where s is 2, 3,         4 or 5, preferably 2, 3 or 4; and -   R^(5b) is selected from hydrogen and deuterium and is preferably     hydrogen.

In an alternative more preferred embodiment,

-   R^(5a) is selected from hydrogen, C₁-C₆-alkyl and fluorinated     C₁-C₆-alkyl; and in case that     -   X is CR⁷R⁸ is further selected from halogen; and is preferably         selected from hydrogen and methyl, or     -   R^(5a) and R⁶ form together a group (CH₂)_(r), where r is 2, 3,         4 or 5, where two hydrogen atoms bound to adjacent CH₂ groups         may be replaced by two radicals     -   R¹¹, where the two radicals R¹¹ form together a group (CH₂)_(t),         where t is 1, 2, 3, 4 or 5, preferably 1, 2 or 3; or     -   R^(5a) and R⁷ form together a group (CH₂)_(s), where s is 2, 3,         4 or 5, preferably 2, 3 or 4; and -   R^(5b) is selected from hydrogen and deuterium and is preferably     hydrogen.

In particular,

-   R^(5a) is hydrogen; and in case that X is CR⁷R⁸, is selected from     hydrogen and methyl and is in particular hydrogen; or     -   R^(5a) and R⁶ form together a group (CH₂)_(r), where r is 3, 4         or 5, where two hydrogen atoms bound to adjacent CH₂ groups may         be replaced by two radicals R¹¹, where the two radicals R¹¹ form         together a group (CH₂)_(t), where t is 1, 2, 3, 4 or 5,         preferably 1, 2 or 3 and specifically 1; or     -   R^(5a) and R⁷ form together a group (CH₂)_(s), where s is 2, 3         or 4, in particular 3; and -   R^(5b) is hydrogen.

In an alternatively preferred embodiment, R^(5a) and R^(5b), together with the carbon atom they are bound to, form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring, where the ring may contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and where the ring may be substituted with one or more substituents R¹¹; and form in particular a 5- or 6-membered saturated or partially unsaturated carbocyclic ring, and where the ring may be substituted with one or more substituents R¹¹.

In one embodiment, X is NR⁶, where R⁶ has one of the general meanings given above, or, in particular, one of the preferred meanings given below.

Preferably, R⁶ is selected from the group consisting of hydrogen, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, —C(═O)R¹⁰, —SO₂R¹⁰, phenyl and benzyl, where the phenyl moiety in the two last-mentioned radicals may carry 1, 2 or 3 radicals R¹¹; or

-   R^(5a) and R⁶, together with the atoms they are bound to, form a 3-,     4-, 5-, 6- or 7-membered saturated, partially unsaturated or     maximally unsaturated heterocyclic ring, where the ring may further     contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups     selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and     where the ring may be substituted with one or more substituents R¹¹;     where R¹⁰ and R¹¹ have one of the general meanings given above, or,     in particular, one of the preferred meanings given below.

In the above group —C(═O)R¹⁰, R⁶, R¹⁰ is preferably selected from C₁-C₄-alkyl and C₁-C₄-alkoxy and more preferably from C₁-C₂-alkyl and tert-butoxy.

In the above group —SO₂R¹⁰, R⁶, R¹⁰ is preferably selected from C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl and phenyl, where phenyl may be substituted with 1, 2, 3, 4 or 5, preferably 1, 2 or 3, in particular 1, radicals R¹¹, where R¹¹ has one of the general meanings given above, or, in particular, one of the preferred meanings given below.

In one more preferred embodiment, R⁶ is —SO₂R¹⁰, where R¹⁰ has one of the general meanings given above or is preferably selected from C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl and phenyl, where phenyl may be substituted with 1, 2, 3, 4 or 5, preferably 1, 2 or 3, in particular 1, radicals R¹¹, where R¹¹ has one of the general meanings given above, or, in particular, one of the preferred meanings given below.

In another preferred embodiment, R⁶ is selected from hydrogen, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₃-C₆-cycloalkyl, fluorinated C₃-C₆-cycloalkyl, C₃-C₆-cycloalkyl-C₁-C₄-alkyl, fluorinated C₃-C₆-cycloalkyl-C₁-C₄-alkyl, C₁-C₄-alkoxy, fluorinated C₁-C₄-alkoxy, —C(═O)R¹⁰, where R¹⁰ is selected from C₁-C₆-alkyl and C₃-C₆-cycloalkyl; phenyl, phenyl-C₁-C₂-alkyl and a 3-, 4-, 5- or 6-membered saturated heterocyclic ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups as ring members, where the cyclic moieties in the three last-mentioned radicals may be substituted with one or more substituents R¹¹.

In another preferred embodiment, R⁶ is selected from C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₃-C₆-cycloalkyl, fluorinated C₃-C₆-cycloalkyl, C₃-C₆-cycloalkyl-C₁-C₂-alkyl, fluorinated C₃-C₆-cycloalkyl-C₁-C₂-alkyl, phenyl, phenyl-C₁-C₂-alkyl and a 3-, 4-, 5- or 6-membered saturated heterocyclic ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups as ring members, where the cyclic moieties in the three last-mentioned radicals may be substituted with one or more substituents R¹¹.

In a more preferred embodiment, R⁶ is phenyl-C₁-C₂-alkyl, and in particular benzyl.

In another more preferred embodiment, R⁶ is selected from C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₃-C₆-cycloalkyl, fluorinated C₃-C₆-cycloalkyl, C₃-C₆-cycloalkyl-C₁-C₂-alkyl and fluorinated C₃-C₆-cycloalkyl-C₁-C₂-alkyl, and in particular from C₁-C₄-alkyl, fluorinated C₁-C₄-alkyl, C₃-C₆-cycloalkyl, fluorinated C₃-C₆-cycloalkyl, C₃-C₆-cycloalkyl-methyl and fluorinated C₃-C₆-cycloalkyl-methyl.

In another more preferred embodiment, R⁶ is a 3-, 4-, 5- or 6-membered saturated heterocyclic ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups as ring members, where the cyclic moieties in the three last-mentioned radicals may be substituted with one or more substituents R¹¹. Even more preferably, R⁶ is a 3-, 4- or 5-membered saturated heterocyclic ring containing 1 or 2 heteroatoms independently selected from N, O and S, where the heterocyclic ring may be substituted with one or two substituents selected from halogen and C₁-C₄-alkyl, and is in particular oxetanyl which may carry one or two substituents selected from halogen and C₁-C₄-alkyl and especially from F.

In another more preferred embodiment, R⁶ is selected from hydrogen, C₁-C₄-alkyl, fluorinated C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkyl-C₁-C₂-alkyl, C₃-C₆-cycloalkylcarbonyl, C₁-C₄-alkoxy, fluorinated C₁-C₄-alkoxy, phenyl-C₁-C₂-alkyl and a 3-, 4-, 5- or 6-membered saturated heterocyclic ring containing 1 or 2 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO and SO₂ as ring members; and is in particular selected from C₁-C₄-alkyl, C₃-C₆-cycloalkyl, C₃-C₆-cycloalkyl-C₁-C₂-alkyl, and a 3-, 4-, 5- or 6-membered saturated heterocyclic ring containing 1 or 2 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO and SO₂ as ring members, where the saturated heterocyclic ring preferably contains 1 heteroatom selected from O and S as ring member. Specifically, R⁶ is selected from C₁-C₄-alkyl, C₃-C₆-cycloalkyl and oxetanyl and very specifically from ethyl, n-propyl, cyclopropyl, cyclobutyl and 3-oxetanyl.

In another more preferred embodiment, R^(5a) and R⁶, together with the atoms they are bound to, form a 3-, 4-, 5-, 6- or 7-membered saturated, partially unsaturated or maximally unsaturated heterocyclic ring, where the ring may further contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and where the ring may be substituted with one or more substituents R¹¹;

where R¹¹ has one of the general meanings given above, or, in particular, one of the preferred meanings given below.

In particular, R^(5a) and R⁶ form together a group (CH₂)_(r), where r is 2, 3, 4 or 5, preferably 2, 3 or 4 or, in particular, 3, 4 or 5. Alternatively, R^(5a) and R⁶ form together a group (CH₂)_(r), where r is 2, 3, 4 or 5 and in particular 3, 4 or 5, where two hydrogen atoms bound to adjacent CH₂ groups may be replaced by two radicals R¹¹, where the two radicals R¹¹ form together a group (CH₂)_(t), where t is 1, 2, 3, 4 or 5, in particular 1, 2 or 3 and specifically 1.

In an alternative embodiment, X is CR⁷R⁸, where R⁷ and R⁸ have one of the general meanings given above, or, in particular, one of the preferred meanings given below.

In case that R⁷ and R⁸, together with the carbon atom they are bound to, form a ring, this ring is spiro-bound to the carbon atom carrying R⁷ and R⁸.

Preferably,

-   R⁷ and R⁸, independently of each other, are selected from the group     consisting of halogen, cyano, nitro, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated     C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl,     C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl,     C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio,     fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated     C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated     C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b),     -   —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b),         C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy,         phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy         and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially         unsaturated or maximally unsaturated ring containing 1, 2, 3 or         4 heteroatoms or heteroatom groups independently selected from         N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the         cyclic moieties in the six last-mentioned radicals may be         substituted with one or more substituents R¹¹; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or     maximally unsaturated ring, where the ring may contain 1, 2, 3 or 4     heteroatoms or heteroatom-containing groups selected from O, S, N,     SO, SO₂, C═O and C═S as ring members, and where the ring may be     substituted with one or more substituents R¹¹; or -   R^(5a) and R⁷, together with the carbon atoms they are bound to,     form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially     unsaturated or maximally unsaturated ring, where the ring may     contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups     selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and     where the ring may be substituted with one or more substituents R¹¹;     in which case R⁸ has one of the above meanings or is deuterium;     where R¹¹ has one of the general meanings given above, or, in     particular, one of the preferred meanings given below.

More preferably,

-   R⁷ and R⁸, independently of each other, are selected from halogen,     cyano, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy, phenyl, phenyl-C₁-C₂-alkyl, benzyloxy and     a 3-, 4-, 5- or 6-membered saturated, partially unsaturated or     maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or     heteroatom groups independently selected from N, O, S, NO, SO, SO₂,     C═O and C═S as ring members, where the cyclic moieties in the four     last-mentioned radicals may be substituted with one or more     substituents R¹¹; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5-, 6- or 7- or 8-membered saturated, partially unsaturated     or maximally unsaturated ring, where the ring may contain 1, 2, 3 or     4 heteroatoms or heteroatom-containing groups selected from O, S, N,     SO, SO₂, C═O and C═S as ring members, and where the ring may be     substituted with one or more substituents R¹¹; or -   R^(5a) and R⁷, together with the carbon atoms they are bound to,     form a 3-, 4-, 5-, 6- or 7-membered saturated, partially unsaturated     or maximally unsaturated ring, where the ring may contain 1, 2, 3 or     4 heteroatoms or heteroatom-containing groups selected from O, S, N,     SO, SO₂, C═O and C═S as ring members, and where the ring may be     substituted with one or more substituents R¹¹;     in which case R⁸ has one of the above meanings or is deuterium; and -   R^(5b) is selected from hydrogen and deuterium and is preferably     hydrogen;     where R¹¹ has one of the general meanings given above, or, in     particular, one of the preferred meanings given below.

Even more preferably,

-   R⁷ and R⁸, independently of each other, are selected from halogen,     cyano, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl and phenyl, or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5-, 6- or 7- or 8-membered saturated, partially unsaturated     or maximally unsaturated ring, where the ring may be substituted     with one or more substituents R¹¹; or -   R⁵ and R⁷ form together a group (CH₂)_(s), where s is 2, 3, 4 or 5,     preferably 2, 3 or 4; in which case R⁸ has one of the above meanings     or is deuterium; and -   R^(5b) is selected from hydrogen and deuterium and is preferably     hydrogen;     where R¹¹ has one of the general meanings given above, or, in     particular, one of the preferred meanings given below.

In particular,

-   R⁸ is selected from halogen, cyano, C₁-C₆-alkyl, fluorinated     C₁-C₆-alkyl and phenyl; and -   R⁷ is selected from C₁-C₆-alkyl and fluorinated C₁-C₆-alkyl,     preferably from methyl and CF₃ and is in particular methyl; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5-, 6- or 7- or 8-membered saturated, partially unsaturated     or maximally unsaturated ring, where the ring may be substituted     with one or more substituents R¹¹; or -   R^(5a) and R⁷ form together a group (CH₂)_(s), where s is 2, 3, 4 or     5, preferably 2, 3 or 4;     in which case R⁸ has one of the above meanings or is deuterium; and -   R^(5b) is selected from hydrogen and deuterium and is preferably     hydrogen;     where R¹¹ has one of the general meanings given above, or, in     particular, one of the preferred meanings given below.

In an alternative particular embodiment,

-   R⁷ is C₁-C₆-alkyl and is in particular methyl; -   R⁸ is selected from hydroxyl, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl,     C₃-C₆-cycloalkyl, fluorinated C₃-C₆-cycloalkyl, C₁-C₆-alkoxy,     fluorinated C₁-C₆-alkoxy and phenyl and in particular from     C₁-C₄-alkyl, fluorinated C₁-C₄-alkyl, C₁-C₄-alkoxy, fluorinated     C₁-C₄-alkoxy and phenyl; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5-, 6- or 7-membered saturated or partially unsaturated     ring, where the ring may be substituted with one or more     substituents R¹¹; or -   R^(5a) and R⁷ form together a group (CH₂)_(s), where s is 2, 3 or 4     and where R⁸ is methyl; and -   R^(5b) is hydrogen.

Specifically,

-   R⁸ is selected from C₁-C₄-alkyl, fluorinated C₁-C₂-alkyl and phenyl     and specifically from methyl, CF₃ and phenyl; and -   R⁷ is methyl; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5- or 6-membered saturated or partially unsaturated ring,     where the ring may be substituted with one or more substituents R¹¹;     or -   R^(5a) and R⁷ form together a group (CH₂)_(s), where s is 3 or 4,     specifically 3;     in which case R⁸ is selected from methyl and deuterium; and -   R^(5b) is selected from hydrogen and deuterium and is specifically     hydrogen;     where R¹¹ has one of the general meanings given above, or, in     particular, one of the preferred meanings given below.

In an alternative specific embodiment,

-   R⁷ is methyl; -   R⁸ is selected from hydroxyl, methyl, ethyl, CF₃, methoxy and     phenyl; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5- or 6-membered saturated or partially unsaturated ring,     where the ring may be substituted with one or more substituents R¹¹;     or -   R^(5a) and R⁷ form together a group (CH₂)_(s), where s is 2, 3 or 4     and in particular and where R⁸ is methyl; and -   R^(5b) is hydrogen.

Very specifically,

-   R⁸ is selected from methyl, CF₃ and phenyl; and -   R⁷ is methyl; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     4, 5- or 6-membered saturated or partially unsaturated ring, where     the ring may be substituted with one or more substituents R¹¹; or     form a 3-membered saturated or partially unsaturated ring, where the     ring may be substituted with one or more substituents R¹¹; or -   R^(5a) and R⁷ form together a group (CH₂)_(s), where s is 3 or 4,     specifically 3;     in which case R⁸ is selected from methyl and deuterium and in     particular methyl; and -   R^(5b) is selected from hydrogen and deuterium and is specifically     hydrogen;     where R¹¹ has one of the general meanings given above, or, in     particular, one of the preferred meanings given below.

In one particular embodiment, the ring formed by R⁷ and R⁸ together with the carbon atom they are bound to is a carbocyclic ring, preferably a saturated or partially unsaturated carbocyclic ring, in particular a saturated carbocyclic ring.

If R⁷ and R⁸, together with the carbon atom they are bound to, form a carbocyclic ring, this is particularly preferably a 4- or 5-membered saturated carbocyclic ring (i.e.

R⁷ and R⁸ form together a group —(CH₂)₃- or —(CH₂)₄-) and in particular a 4-membered saturated carbocyclic ring (i.e. R⁷ and R⁸ form together a group —(CH₂)₃-), where the ring may be substituted with one or more substituents R¹¹. Specifically, the ring is not substituted. Alternatively, the carbocyclic ring is 3-membered (i.e. R⁷ and R⁸ form together a group —(CH₂)₂—)—), where the ring may be substituted with one or more substituents R¹¹. Specifically, the ring is not substituted.

In an alternative particular embodiment, the ring formed by R⁷ and R⁸ together with the carbon atom they are bound to is a heterocyclic ring containing 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups selected from O, S, N, SO and SO₂ as ring members, preferably containing 1 or 2 heteroatoms or heteroatom-containing groups selected from O, S, N, SO and SO₂ as ring members. Preferably, the heterocyclic ring is 3-, 4-, 5- or 6-membered and saturated and may carry one or more substituents R¹¹. In particular, the heterocyclic ring is oxetanyl which may carry one or more substituents R¹¹.

Specifically, R⁷ and R⁸, together with the carbon atom they are bound to, form a 3- or 4-membered saturated carbocyclic ring (i.e. R⁷ and R⁸ form together a group —(CH₂)₂— or —(CH₂)₃—) and in particular a 4-membered saturated carbocyclic ring (i.e. R⁷ and R⁸ form together a group —(CH₂)₃—); the ring not being substituted.

In a preferred embodiment, each R⁹ is independently selected from halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₃-C₆-cycloalkyl, fluorinated C₃-C₆-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy and a 3-, 4-, 5- or 6-membered saturated heterocyclic ring containing 1 or 2 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO and SO₂ as ring members, where the heterocyclic ring may be substituted with one or more substituents R¹¹. The heterocyclic ring is specifically oxetanyl.

More preferably, each R⁹ is independently selected from halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy, even more preferably from halogen, cyano, C₁-C₄-alkyl, fluorinated C₁-C₄-alkyl, C₁-C₄-alkoxy and fluorinated C₁-C₄-alkoxy, and is in particular selected from halogen, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₃-C₆-cycloalkyl and C₁-C₆-alkoxy, more particularly from halogen, C₁-C₆-alkyl and C₁-C₆-alkoxy, and is specifically halogen, especially F or Cl, and more specifically F.

In case that X is NR⁶, in alternatively more preferred embodiment, each R⁹ is independently selected from halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₃-C₆-cycloalkyl, fluorinated C₃-C₆-cycloalkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy, even more preferably from halogen, C₁-C₆-alkyl and C₃-C₆-cycloalkyl, and in particular from halogen and C₁-C₆-alkyl.

In a preferred embodiment, R¹⁰ is selected from hydrogen, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), phenyl, phenyl-C₁-C₂-alkyl, phenoxy, benzyloxy and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the cyclic moieties in the five last-mentioned radicals may be substituted with one or more substituents R¹¹, where R¹¹, R^(12a) and R^(12b) have one of the general meanings given above, or, in particular, one of the preferred meanings given below. More preferably, R¹⁰ is selected from hydrogen, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy, and even more preferably from C₁-C₄-alkyl and C₁-C₄-alkoxy. In particular, R¹⁰ is selected from C₁-C₂-alkyl and tert-butoxy.

In a preferred embodiment, each R¹¹ is independently selected from halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy, and is in particular halogen or C₁-C₄-alkyl. Alternatively, two radicals R¹¹ bound on adjacent ring atoms form together a group (CH₂)_(t), where t is 1, 2, 3, 4 or 5 and in particular 1, 2 or 3.

In a preferred embodiment, R^(12a) and R^(12b), independently of each other and independently of each occurrence, are selected from hydrogen, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkylcarbonyl, fluorinated C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, fluorinated C₁-C₆-alkoxycarbonyl, phenyl and benzyl, where the phenyl moieties in the two last-mentioned radicals may carry 1, 2 or 3 substituents selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy; or,

if R^(12a) and R^(12b) are bound to the same nitrogen atom, together with this nitrogen atom may form a 3-, 4-, 5-, 6- or 7-membered saturated, partially unsaturated or maximally unsaturated heterocyclic ring, where the ring may further contain 1 or 2 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and where the ring may be substituted with one or more substituents selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy.

More preferably, R^(12a) and R^(12b), independently of each other and independently of each occurrence, are selected from hydrogen, C₁-C₆-alkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl and benzyl, where the phenyl moiety in the last-mentioned radical may carry 1, 2 or 3 substituents selected from halogen, cyano nitro, C₁-C₄-alkyl, fluorinated C₁-C₄-alkyl, C₁-C₄-alkoxy and fluorinated C₁-C₄-alkoxy; or, if R^(12a) and R^(12b) are bound to the same nitrogen atom, together with this nitrogen atom may form a 5- or 6-membered saturated or aromatic heterocyclic ring, where the ring may further contain 1 or 2 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂ and C═O as ring members, and where the ring may be substituted with 1 or 2 substituents selected from halogen, cyano nitro, C₁-C₄-alkyl, fluorinated C₁-C₄-alkyl, C₁-C₄-alkoxy and fluorinated C₁-C₄-alkoxy.

In particular, R^(12a) and R^(12b), independently of each other and independently of each occurrence, are selected from hydrogen and C₁-C₆-alkyl.

In a preferred embodiment, a is 0 or 1 and in particular 0.

In a particular embodiment, a is 1 and R² is bound in 3-position to the nitrogen ring atom carrying R¹ (this is for the example the position of R^(2b) in below formula I.2).

In a preferred embodiment, b is 0, 1 or 2 and in particular 0 or 1.

In a preferred embodiment, n is 1.

In a particular embodiment, the compound of formula I is a compound of formula I.1

wherein X, R^(5a), R^(5b), R⁹ and b have one of the above general, or, in particular, one of the above preferred meanings.

In a specific embodiment, the compound of formula I is a compound of formula I.1.1

wherein

-   R^(9a) is selected from H, halogen, C₁-C₄-alkyl, fluorinated     C₁-C₄-alkyl, C₃-C₆-cycloalkyl and fluorinated C₃-C₆-cycloalkyl,     especially from H or F; and -   R^(5a), R^(5b), R⁶, R⁹ and b have one of the above general, or, in     particular, one of the above preferred meanings.

In another specific embodiment, the compound of formula I is a compound of formula I.1.2

wherein

-   R⁷ is selected from C₁-C₄-alkyl and fluorinated C₁-C₄-alkyl; -   R⁸ is selected from C₁-C₄-alkyl, fluorinated C₁-C₄-alkyl,     C₁-C₄-alkoxy, fluorinated C₁-C₄-alkoxy and phenyl; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5-, 6- or 7-membered, in particular a 3- or 4-membered     saturated or partially unsaturated ring, especially a saturated     carbocyclic ring, where the ring may be substituted with one or more     substituents R¹¹, and form especially a 3- or 4-membered saturated     carbocyclic ring; -   R^(9a) is H, Cl, F or methyl, especially H, Cl or F; and -   R⁹ and b have one of the above general, or, in particular, one of     the above preferred meanings.

In an alternative embodiment, in compounds I.1.2,

-   R⁷ is selected from C₁-C₄-alkyl and fluorinated C₁-C₄-alkyl,     preferably from methyl and CF₃, and is in particular methyl; -   R⁸ is selected from C₁-C₄-alkyl and fluorinated C₁-C₄-alkyl, and     preferably from methyl and CF₃; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5-, 6- or 7-membered saturated or partially unsaturated     ring, where the ring may be substituted with one or more     substituents R¹¹, and form preferably a 5- or 6-membered saturated     or partially unsaturated ring; -   R^(9a) is H or F; and -   R⁹ and b have one of the above general, or, in particular, one of     the above preferred meanings.

In another specific embodiment, the compound of formula I is a compound of formula I.1.3

wherein R⁸ is selected from deuterium, F, Cl, CN and CH₃, in particular from deuterium, F, Cl and CN.

Among these, preference is given to the trans compounds, i.e. of formula I.1.3-trans:

wherein R⁸ is selected from deuterium, F, Cl, CN and CH₃, in particular from deuterium, F, Cl and CN.

In another particular embodiment, the compound of formula I is a compound of formula I.2

wherein X, R^(5a), R^(5b), R⁹ and b have one of the above general, or, in particular, one of the above preferred meanings.

In another particular embodiment, the compound of formula I is a compound of formula I.2.1

wherein

-   R^(2a), R^(2b) and R^(3a), independently of each other, are selected     from hydrogen and methyl; and where in particular at most one of     R^(2a), R^(2b) and R^(3a) is methyl; -   R^(9a) is selected from H, halogen, C₁-C₄-alkyl, fluorinated     C₁-C₄-alkyl, C₃-C₆-cycloalkyl and fluorinated C₃-C₆-cycloalkyl; and -   R^(5a), R^(5b), R⁶, R⁹ and b have one of the above general, or, in     particular, one of the above preferred meanings.

In particular, in compounds I.2.1,

-   R^(9a) is H or F; and -   R^(5a), R^(5b), R⁶, R⁹ and b have one of the above general, or, in     particular, one of the above preferred meanings.

In particular, in compounds 1.2.1, R^(2b) is methyl and R^(2a) and R^(3a) are hydrogen.

In another particular embodiment, the compound of formula I is a compound of formula I.2.2

wherein

-   R^(2a), R^(2b), R^(3a) and R^(5a), independently of each other, are     selected from hydrogen, methyl and ethyl, in particular from     hydrogen and methyl; -   R⁷ is selected from C₁-C₄-alkyl and fluorinated C₁-C₄-alkyl, in     particular from methyl and CF₃, and is especially methyl; -   R⁸ is selected from C₁-C₄-alkyl, fluorinated C₁-C₄-alkyl,     C₁-C₄-alkoxy, fluorinated C₁-C₄-alkoxy and phenyl; and in particular     from methyl and CF₃; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5-, 6- or 7-membered, in particular a 3- or 4-membered     saturated or partially unsaturated, especially a saturated     carbocyclic ring, ring, where the ring may be substituted with one     or more substituents R¹¹, and form especially a 3- or 4-membered     saturated carbocyclic ring; -   R^(9a) is H, Cl, F or methyl, especially H, Cl or F; and -   R⁹ and b have one of the above general, or, in particular, one of     the above preferred meanings.

In particular, in compound 1.2.2,

-   R^(2a), R^(2b), R^(3a) and R^(5a), independently of each other, are     selected from hydrogen and methyl; -   R⁷ is selected from C₁-C₄-alkyl and fluorinated C₁-C₄-alkyl,     preferably from methyl and CF₃, and is in particular methyl; -   R⁸ is selected from C₁-C₄-alkyl and fluorinated C₁-C₄-alkyl, and     preferably from methyl and CF₃; or -   R⁷ and R⁸, together with the carbon atom they are bound to, form a     3-, 4-, 5-, 6- or 7-membered saturated or partially unsaturated     ring, where the ring may be substituted with one or more     substituents R¹¹; -   R^(9a) is H or F; and -   R⁹ and b have one of the above general, or, in particular, one of     the above preferred meanings.

In particular, in compound 1.2.2, R^(2b) is methyl and R^(2a), R^(3a) and R^(5a) are hydrogen. In the above formulae I.1.1, I.1.2, I.2.1 and I.2.2, (b-1) is preferably 0.

Preferably, in the above formulae I.1.2, I.2.1 and I.2.2, R^(2a), R^(2b), R^(3a) and R^(5a) are selected from hydrogen and methyl, with the proviso that at most two, preferably at most one, of the substituents R^(2a), R^(2b), R^(3a) and R^(5a) are methyl. In particular, R^(2b) is hydrogen and R^(2a), R^(3a) and R^(5a) are selected from hydrogen and methyl, with the proviso that at most two, preferably at most one, of the substituents R^(2a), R^(3a) and R^(5a) are methyl. However, more particularly, R^(2b) is hydrogen or methyl, especially methyl, and R^(2a), R^(3a) and R^(5a) are hydrogen (if the latter does not form a ring together with R⁶ or R⁷ and the atoms they are bond to).

Preferably, in the above formulae I.2, I.2.1 and I.2.2, R⁷ and R⁸, together with the carbon atom they are bound to, form a 3, 4-, 5- or 6-membered saturated or partially unsaturated carbocyclic ring, preferably a 3, 4- or 5-membered saturated carbocyclic ring, in particular a 4-membered saturated carbocyclic ring, where the ring may be substituted with one or more substituents R¹¹.

Examples of preferred compounds are compounds of the following formulae I.a to I.ii, where the variables have one of the general or preferred meanings given above.

Examples of preferred compounds are the individual compounds compiled in the tables 1 to 36 below. Moreover, the meanings mentioned below for the individual variables in the tables are per se, independently of the combination in which they are mentioned, a particularly preferred embodiment of the substituents in question.

Table 1

Compounds of the formula I.a in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 2

Compounds of the formula I.b in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 3

Compounds of the formula I.c in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 4

Compounds of the formula I.d in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 5

Compounds of the formula I.e in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 6

Compounds of the formula I.f in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 7

Compounds of the formula I.g in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 8

Compounds of the formula I.h in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 9

Compounds of the formula I.i in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 10

Compounds of the formula I.j in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 11

Compounds of the formula I.k in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 12

Compounds of the formula I.1 in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 13

Compounds of the formula I.m in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 14

Compounds of the formula I.n in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 15

Compounds of the formula I.o in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 16

Compounds of the formula I.p in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 17

Compounds of the formula I.q in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 18

Compounds of the formula I.r in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 19

Compounds of the formula I.s in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 20

Compounds of the formula I.t in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 21

Compounds of the formula I.u in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 22

Compounds of the formula I.v in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 23

Compounds of the formula I.w in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 24

Compounds of the formula I.x in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 25

Compounds of the formula I.y in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 26

Compounds of the formula I.z in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 27

Compounds of the formula I.zz in which the combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) for a compound corresponds in each case to one row of Table B.

Table 28

Compounds of the formula I.aa in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 29

Compounds of the formula I.bb in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 30

Compounds of the formula I.cc in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 31

Compounds of the formula I.dd in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 32

Compounds of the formula I.ee in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 33

Compounds of the formula I.ff in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 34

Compounds of the formula I.gg in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 35

Compounds of the formula I.hh in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

Table 36

Compounds of the formula I.ii in which the combination of R^(5a), R^(5b), R⁶ and R^(9a) for a compound corresponds in each case to one row of Table A.

TABLE A No. R^(9a) R^(5b) R^(5a) R⁶ A-1 H H H —SO₂—CH₃ A-2 F H H —SO₂—CH₃ A-3 Cl H H —SO₂—CH₃ A-4 Br H H —SO₂—CH₃ A-5 CH₃ H H —SO₂—CH₃ A-6 CF₃ H H —SO₂—CH₃ A-7 OCH₃ H H —SO₂—CH₃ A-8 OCF₃ H H —SO₂—CH₃ A-9 cyclopropyl H H —SO₂—CH₃ A-10 cyclobutyl H H —SO₂—CH₃ A-11 cyclopentyl H H —SO₂—CH₃ A-12 cyclohexyl H H —SO₂—CH₃ A-13 H CH₃ H —SO₂—CH₃ A-14 F CH₃ H —SO₂—CH₃ A-15 Cl CH₃ H —SO₂—CH₃ A-16 Br CH₃ H —SO₂—CH₃ A-17 CH₃ CH₃ H —SO₂—CH₃ A-18 CF₃ CH₃ H —SO₂—CH₃ A-19 OCH₃ CH₃ H —SO₂—CH₃ A-20 OCF₃ CH₃ H —SO₂—CH₃ A-21 cyclopropyl CH₃ H —SO₂—CH₃ A-22 cyclobutyl CH₃ H —SO₂—CH₃ A-23 cyclopentyl CH₃ H —SO₂—CH₃ A-24 cyclohexyl CH₃ H —SO₂—CH₃ A-25 H CH₃ CH₃ —SO₂—CH₃ A-26 F CH₃ CH₃ —SO₂—CH₃ A-27 Cl CH₃ CH₃ —SO₂—CH₃ A-28 Br CH₃ CH₃ —SO₂—CH₃ A-29 CH₃ CH₃ CH₃ —SO₂—CH₃ A-30 CF₃ CH₃ CH₃ —SO₂—CH₃ A-31 OCH₃ CH₃ CH₃ —SO₂—CH₃ A-32 OCF₃ CH₃ CH₃ —SO₂—CH₃ A-33 cyclopropyl CH₃ CH₃ —SO₂—CH₃ A-34 cyclobutyl CH₃ CH₃ —SO₂—CH₃ A-35 cyclopentyl CH₃ CH₃ —SO₂—CH₃ A-36 cyclohexyl CH₃ CH₃ —SO₂—CH₃ A-37 H H H —SO₂—CH₂CH₃ A-38 F H H —SO₂—CH₂CH₃ A-39 Cl H H —SO₂—CH₂CH₃ A-40 Br H H —SO₂—CH₂CH₃ A-41 CH₃ H H —SO₂—CH₂CH₃ A-42 CF₃ H H —SO₂—CH₂CH₃ A-43 OCH₃ H H —SO₂—CH₂CH₃ A-44 OCF₃ H H —SO₂—CH₂CH₃ A-45 cyclopropyl H H —SO₂—CH₂CH₃ A-46 cyclobutyl H H —SO₂—CH₂CH₃ A-47 cyclopentyl H H —SO₂—CH₂CH₃ A-48 cyclohexyl H H —SO₂—CH₂CH₃ A-49 H CH₃ H —SO₂—CH₂CH₃ A-50 F CH₃ H —SO₂—CH₂CH₃ A-51 Cl CH₃ H —SO₂—CH₂CH₃ A-52 Br CH₃ H —SO₂—CH₂CH₃ A-53 CH₃ CH₃ H —SO₂—CH₂CH₃ A-54 CF₃ CH₃ H —SO₂—CH₂CH₃ A-55 OCH₃ CH₃ H —SO₂—CH₂CH₃ A-56 OCF₃ CH₃ H —SO₂—CH₂CH₃ A-57 cyclopropyl CH₃ H —SO₂—CH₂CH₃ A-58 cyclobutyl CH₃ H —SO₂—CH₂CH₃ A-59 cyclopentyl CH₃ H —SO₂—CH₂CH₃ A-60 cyclohexyl CH₃ H —SO₂—CH₂CH₃ A-61 H CH₃ CH₃ —SO₂—CH₂CH₃ A-62 F CH₃ CH₃ —SO₂—CH₂CH₃ A-63 Cl CH₃ CH₃ —SO₂—CH₂CH₃ A-64 Br CH₃ CH₃ —SO₂—CH₂CH₃ A-65 CH₃ CH₃ CH₃ —SO₂—CH₂CH₃ A-66 CF₃ CH₃ CH₃ —SO₂—CH₂CH₃ A-67 OCH₃ CH₃ CH₃ —SO₂—CH₂CH₃ A-68 OCF₃ CH₃ CH₃ —SO₂—CH₂CH₃ A-69 cyclopropyl CH₃ CH₃ —SO₂—CH₂CH₃ A-70 cyclobutyl CH₃ CH₃ —SO₂—CH₂CH₃ A-71 cyclopentyl CH₃ CH₃ —SO₂—CH₂CH₃ A-72 cyclohexyl CH₃ CH₃ —SO₂—CH₂CH₃ A-73 H H H —SO₂—CF₃ A-74 F H H —SO₂—CF₃ A-75 Cl H H —SO₂—CF₃ A-76 Br H H —SO₂—CF₃ A-77 CH₃ H H —SO₂—CF₃ A-78 CF₃ H H —SO₂—CF₃ A-79 OCH₃ H H —SO₂—CF₃ A-80 OCF₃ H H —SO₂—CF₃ A-81 cyclopropyl H H —SO₂—CF₃ A-82 cyclobutyl H H —SO₂—CF₃ A-83 cyclopentyl H H —SO₂—CF₃ A-84 cyclohexyl H H —SO₂—CF₃ A-85 H CH₃ H —SO₂—CF₃ A-86 F CH₃ H —SO₂—CF₃ A-87 Cl CH₃ H —SO₂—CF₃ A-88 Br CH₃ H —SO₂—CF₃ A-89 CH₃ CH₃ H —SO₂—CF₃ A-90 CF₃ CH₃ H —SO₂—CF₃ A-91 OCH₃ CH₃ H —SO₂—CF₃ A-92 OCF₃ CH₃ H —SO₂—CF₃ A-93 cyclopropyl CH₃ H —SO₂—CF₃ A-94 cyclobutyl CH₃ H —SO₂—CF₃ A-95 cyclopentyl CH₃ H —SO₂—CF₃ A-96 cyclohexyl CH₃ H —SO₂—CF₃ A-97 H CH₃ CH₃ —SO₂—CF₃ A-98 F CH₃ CH₃ —SO₂—CF₃ A-99 Cl CH₃ CH₃ —SO₂—CF₃ A-100 Br CH₃ CH₃ —SO₂—CF₃ A-101 CH₃ CH₃ CH₃ —SO₂—CF₃ A-102 CF₃ CH₃ CH₃ —SO₂—CF₃ A-103 OCH₃ CH₃ CH₃ —SO₂—CF₃ A-104 OCF₃ CH₃ CH₃ —SO₂—CF₃ A-105 cyclopropyl CH₃ CH₃ —SO₂—CF₃ A-106 cyclobutyl CH₃ CH₃ —SO₂—CF₃ A-107 cyclopentyl CH₃ CH₃ —SO₂—CF₃ A-108 cyclohexyl CH₃ CH₃ —SO₂—CF₃ A-109 H H H —SO₂—C₆H₅* A-110 F H H —SO₂—C₆H₅ A-111 Cl H H —SO₂—C₆H₅ A-112 Br H H —SO₂—C₆H₅ A-113 CH₃ H H —SO₂—C₆H₅ A-114 CF₃ H H —SO₂—C₆H₅ A-115 OCH₃ H H —SO₂—C₆H₅ A-116 OCF₃ H H —SO₂—C₆H₅ A-117 cyclopropyl H H —SO₂—C₆H₅ A-118 cyclobutyl H H —SO₂—C₆H₅ A-119 cyclopentyl H H —SO₂—C₆H₅ A-120 cyclohexyl H H —SO₂—C₆H₅ A-121 H CH₃ H —SO₂—C₆H₅ A-122 F CH₃ H —SO₂—C₆H₅ A-123 Cl CH₃ H —SO₂—C₆H₅ A-124 Br CH₃ H —SO₂—C₆H₅ A-125 CH₃ CH₃ H —SO₂—C₆H₅ A-126 CF₃ CH₃ H —SO₂—C₆H₅ A-127 OCH₃ CH₃ H —SO₂—C₆H₅ A-128 OCF₃ CH₃ H —SO₂—C₆H₅ A-129 cyclopropyl CH₃ H —SO₂—C₆H₅ A-130 cyclobutyl CH₃ H —SO₂—C₆H₅ A-131 cyclopentyl CH₃ H —SO₂—C₆H₅ A-132 cyclohexyl CH₃ H —SO₂—C₆H₅ A-133 H CH₃ CH₃ —SO₂—C₆H₅ A-134 F CH₃ CH₃ —SO₂—C₆H₅ A-135 Cl CH₃ CH₃ —SO₂—C₆H₅ A-136 Br CH₃ CH₃ —SO₂—C₆H₅ A-137 CH₃ CH₃ CH₃ —SO₂—C₆H₅ A-138 CF₃ CH₃ CH₃ —SO₂—C₆H₅ A-139 OCH₃ CH₃ CH₃ —SO₂—C₆H₅ A-140 OCF₃ CH₃ CH₃ —SO₂—C₆H₅ A-141 cyclopropyl CH₃ CH₃ —SO₂—C₆H₅ A-142 cyclobutyl CH₃ CH₃ —SO₂—C₆H₅ A-143 cyclopentyl CH₃ CH₃ —SO₂—C₆H₅ A-144 cyclohexyl CH₃ CH₃ —SO₂—C₆H₅ A-145 H H H —SO₂—C₆H₄CH₃** A-146 F H H —SO₂—C₆H₄CH₃ A-147 Cl H H —SO₂—C₆H₄CH₃ A-148 Br H H —SO₂—C₆H₄CH₃ A-149 CH₃ H H —SO₂—C₆H₄CH₃ A-150 CF₃ H H —SO₂—C₆H₄CH₃ A-151 OCH₃ H H —SO₂—C₆H₄CH₃ A-152 OCF₃ H H —SO₂—C₆H₄CH₃ A-153 cyclopropyl H H —SO₂—C₆H₄CH₃ A-154 cyclobutyl H H —SO₂—C₆H₄CH₃ A-155 cyclopentyl H H —SO₂—C₆H₄CH₃ A-156 cyclohexyl H H —SO₂—C₆H₄CH₃ A-157 H CH₃ H —SO₂—C₆H₄CH₃ A-158 F CH₃ H —SO₂—C₆H₄CH₃ A-159 Cl CH₃ H —SO₂—C₆H₄CH₃ A-160 Br CH₃ H —SO₂—C₆H₄CH₃ A-161 CH₃ CH₃ H —SO₂—C₆H₄CH₃ A-162 CF₃ CH₃ H —SO₂—C₆H₄CH₃ A-163 OCH₃ CH₃ H —SO₂—C₆H₄CH₃ A-164 OCF₃ CH₃ H —SO₂—C₆H₄CH₃ A-165 cyclopropyl CH₃ H —SO₂—C₆H₄CH₃ A-166 cyclobutyl CH₃ H —SO₂—C₆H₄CH₃ A-167 cyclopentyl CH₃ H —SO₂—C₆H₄CH₃ A-168 cyclohexyl CH₃ H —SO₂—C₆H₄CH₃ A-169 H CH₃ CH₃ —SO₂—C₆H₄CH₃ A-170 F CH₃ CH₃ —SO₂—C₆H₄CH₃ A-171 Cl CH₃ CH₃ —SO₂—C₆H₄CH₃ A-172 Br CH₃ CH₃ —SO₂—C₆H₄CH₃ A-173 CH₃ CH₃ CH₃ —SO₂—C₆H₄CH₃ A-174 CF₃ CH₃ CH₃ —SO₂—C₆H₄CH₃ A-175 OCH₃ CH₃ CH₃ —SO₂—C₆H₄CH₃ A-176 OCF₃ CH₃ CH₃ —SO₂—C₆H₄CH₃ A-177 cyclopropyl CH₃ CH₃ —SO₂—C₆H₄CH₃ A-178 cyclobutyl CH₃ CH₃ —SO₂—C₆H₄CH₃ A-179 cyclopentyl CH₃ CH₃ —SO₂—C₆H₄CH₃ A-180 cyclohexyl CH₃ CH₃ —SO₂—C₆H₄CH₃ A-181 H H H benzyl A-182 F H H benzyl A-183 Cl H H benzyl A-184 Br H H benzyl A-185 CH₃ H H benzyl A-186 CF₃ H H benzyl A-187 OCH₃ H H benzyl A-188 OCF₃ H H benzyl A-189 cyclopropyl H H benzyl A-190 cyclobutyl H H benzyl A-191 cyclopentyl H H benzyl A-192 cyclohexyl H H benzyl A-193 H CH₃ H benzyl A-194 F CH₃ H benzyl A-195 Cl CH₃ H benzyl A-196 Br CH₃ H benzyl A-197 CH₃ CH₃ H benzyl A-198 CF₃ CH₃ H benzyl A-199 OCH₃ CH₃ H benzyl A-200 OCF₃ CH₃ H benzyl A-201 cyclopropyl CH₃ H benzyl A-202 cyclobutyl CH₃ H benzyl A-203 cyclopentyl CH₃ H benzyl A-204 cyclohexyl CH₃ H benzyl A-205 H CH₃ CH₃ benzyl A-206 F CH₃ CH₃ benzyl A-207 Cl CH₃ CH₃ benzyl A-208 Br CH₃ CH₃ benzyl A-209 CH₃ CH₃ CH₃ benzyl A-210 CF₃ CH₃ CH₃ benzyl A-211 OCH₃ CH₃ CH₃ benzyl A-212 OCF₃ CH₃ CH₃ benzyl A-213 cyclopropyl CH₃ CH₃ benzyl A-214 cyclobutyl CH₃ CH₃ benzyl A-215 cyclopentyl CH₃ CH₃ benzyl A-216 cyclohexyl CH₃ CH₃ benzyl A-217 H H H H A-218 F H H H A-219 Cl H H H A-220 Br H H H A-221 CH₃ H H H A-222 CF₃ H H H A-223 OCH₃ H H H A-224 OCF₃ H H H A-225 cyclopropyl H H H A-226 cyclobutyl H H H A-227 cyclopentyl H H H A-228 cyclohexyl H H H A-229 H CH₃ H H A-230 F CH₃ H H A-231 Cl CH₃ H H A-232 Br CH₃ H H A-233 CH₃ CH₃ H H A-234 CF₃ CH₃ H H A-235 OCH₃ CH₃ H H A-236 OCF₃ CH₃ H H A-237 cyclopropyl CH₃ H H A-238 cyclobutyl CH₃ H H A-239 cyclopentyl CH₃ H H A-240 cyclohexyl CH₃ H H A-241 H CH₃ CH₃ H A-242 F CH₃ CH₃ H A-243 Cl CH₃ CH₃ H A-244 Br CH₃ CH₃ H A-245 CH₃ CH₃ CH₃ H A-246 CF₃ CH₃ CH₃ H A-247 OCH₃ CH₃ CH₃ H A-248 OCF₃ CH₃ CH₃ H A-249 cyclopropyl CH₃ CH₃ H A-250 cyclobutyl CH₃ CH₃ H A-251 cyclopentyl CH₃ CH₃ H A-252 cyclohexyl CH₃ CH₃ H A-253 H H H CH₃ A-254 F H H CH₃ A-255 Cl H H CH₃ A-256 Br H H CH₃ A-257 CH₃ H H CH₃ A-258 CF₃ H H CH₃ A-259 OCH₃ H H CH₃ A-260 OCF₃ H H CH₃ A-261 cyclopropyl H H CH₃ A-262 cyclobutyl H H CH₃ A-263 cyclopentyl H H CH₃ A-264 cyclohexyl H H CH₃ A-265 H CH₃ H CH₃ A-266 F CH₃ H CH₃ A-267 Cl CH₃ H CH₃ A-268 Br CH₃ H CH₃ A-269 CH₃ CH₃ H CH₃ A-270 CF₃ CH₃ H CH₃ A-271 OCH₃ CH₃ H CH₃ A-272 OCF₃ CH₃ H CH₃ A-273 cyclopropyl CH₃ H CH₃ A-274 cyclobutyl CH₃ H CH₃ A-275 cyclopentyl CH₃ H CH₃ A-276 cyclohexyl CH₃ H CH₃ A-277 H CH₃ CH₃ CH₃ A-278 F CH₃ CH₃ CH₃ A-279 Cl CH₃ CH₃ CH₃ A-280 Br CH₃ CH₃ CH₃ A-281 CH₃ CH₃ CH₃ CH₃ A-282 CF₃ CH₃ CH₃ CH₃ A-283 OCH₃ CH₃ CH₃ CH₃ A-284 OCF₃ CH₃ CH₃ CH₃ A-285 cyclopropyl CH₃ CH₃ CH₃ A-286 cyclobutyl CH₃ CH₃ CH₃ A-287 cyclopentyl CH₃ CH₃ CH₃ A-288 cyclohexyl CH₃ CH₃ CH₃ A-289 H H H C₂H₅ A-290 F H H C₂H₅ A-291 Cl H H C₂H₅ A-292 Br H H C₂H₅ A-293 CH₃ H H C₂H₅ A-294 CF₃ H H C₂H₅ A-295 OCH₃ H H C₂H₅ A-296 OCF₃ H H C₂H₅ A-297 cyclopropyl H H C₂H₅ A-298 cyclobutyl H H C₂H₅ A-299 cyclopentyl H H C₂H₅ A-300 cyclohexyl H H C₂H₅ A-301 H CH₃ H C₂H₅ A-302 F CH₃ H C₂H₅ A-303 Cl CH₃ H C₂H₅ A-304 Br CH₃ H C₂H₅ A-305 CH₃ CH₃ H C₂H₅ A-306 CF₃ CH₃ H C₂H₅ A-307 OCH₃ CH₃ H C₂H₅ A-308 OCF₃ CH₃ H C₂H₅ A-309 cyclopropyl CH₃ H C₂H₅ A-310 cyclobutyl CH₃ H C₂H₅ A-311 cyclopentyl CH₃ H C₂H₅ A-312 cyclohexyl CH₃ H C₂H₅ A-313 H CH₃ CH₃ C₂H₅ A-314 F CH₃ CH₃ C₂H₅ A-315 Cl CH₃ CH₃ C₂H₅ A-316 Br CH₃ CH₃ C₂H₅ A-317 CH₃ CH₃ CH₃ C₂H₅ A-318 CF₃ CH₃ CH₃ C₂H₅ A-319 OCH₃ CH₃ CH₃ C₂H₅ A-320 OCF₃ CH₃ CH₃ C₂H₅ A-321 cyclopropyl CH₃ CH₃ C₂H₅ A-322 cyclobutyl CH₃ CH₃ C₂H₅ A-323 cyclopentyl CH₃ CH₃ C₂H₅ A-324 cyclohexyl CH₃ CH₃ C₂H₅ A-325 H H H n-propyl A-326 F H H n-propyl A-327 Cl H H n-propyl A-328 Br H H n-propyl A-329 CH₃ H H n-propyl A-330 CF₃ H H n-propyl A-331 OCH₃ H H n-propyl A-332 OCF₃ H H n-propyl A-333 cyclopropyl H H n-propyl A-334 cyclobutyl H H n-propyl A-335 cyclopentyl H H n-propyl A-336 cyclohexyl H H n-propyl A-337 H CH₃ H n-propyl A-338 F CH₃ H n-propyl A-339 Cl CH₃ H n-propyl A-340 Br CH₃ H n-propyl A-341 CH₃ CH₃ H n-propyl A-342 CF₃ CH₃ H n-propyl A-343 OCH₃ CH₃ H n-propyl A-344 OCF₃ CH₃ H n-propyl A-345 cyclopropyl CH₃ H n-propyl A-346 cyclobutyl CH₃ H n-propyl A-347 cyclopentyl CH₃ H n-propyl A-348 cyclohexyl CH₃ H n-propyl A-349 H CH₃ CH₃ n-propyl A-350 F CH₃ CH₃ n-propyl A-351 Cl CH₃ CH₃ n-propyl A-352 Br CH₃ CH₃ n-propyl A-353 CH₃ CH₃ CH₃ n-propyl A-354 CF₃ CH₃ CH₃ n-propyl A-355 OCH₃ CH₃ CH₃ n-propyl A-356 OCF₃ CH₃ CH₃ n-propyl A-357 cyclopropyl CH₃ CH₃ n-propyl A-358 cyclobutyl CH₃ CH₃ n-propyl A-359 cyclopentyl CH₃ CH₃ n-propyl A-360 cyclohexyl CH₃ CH₃ n-propyl A-361 H H H isopropyl A-362 F H H isopropyl A-363 Cl H H isopropyl A-364 Br H H isopropyl A-365 CH₃ H H isopropyl A-366 CF₃ H H isopropyl A-367 OCH₃ H H isopropyl A-368 OCF₃ H H isopropyl A-369 cyclopropyl H H isopropyl A-370 cyclobutyl H H isopropyl A-371 cyclopentyl H H isopropyl A-372 cyclohexyl H H isopropyl A-373 H CH₃ H isopropyl A-374 F CH₃ H isopropyl A-375 Cl CH₃ H isopropyl A-376 Br CH₃ H isopropyl A-377 CH₃ CH₃ H isopropyl A-378 CF₃ CH₃ H isopropyl A-379 OCH₃ CH₃ H isopropyl A-380 OCF₃ CH₃ H isopropyl A-381 cyclopropyl CH₃ H isopropyl A-382 cyclobutyl CH₃ H isopropyl A-383 cyclopentyl CH₃ H isopropyl A-384 cyclohexyl CH₃ H isopropyl A-385 H CH₃ CH₃ isopropyl A-386 F CH₃ CH₃ isopropyl A-387 Cl CH₃ CH₃ isopropyl A-388 Br CH₃ CH₃ isopropyl A-389 CH₃ CH₃ CH₃ isopropyl A-390 CF₃ CH₃ CH₃ isopropyl A-391 OCH₃ CH₃ CH₃ isopropyl A-392 OCF₃ CH₃ CH₃ isopropyl A-393 cyclopropyl CH₃ CH₃ isopropyl A-394 cyclobutyl CH₃ CH₃ isopropyl A-395 cyclopentyl CH₃ CH₃ isopropyl A-396 cyclohexyl CH₃ CH₃ isopropyl A-397 H H H n-butyl A-398 F H H n-butyl A-399 Cl H H n-butyl A-400 Br H H n-butyl A-401 CH₃ H H n-butyl A-402 CF₃ H H n-butyl A-403 OCH₃ H H n-butyl A-404 OCF₃ H H n-butyl A-405 cyclopropyl H H n-butyl A-406 cyclobutyl H H n-butyl A-407 cyclopentyl H H n-butyl A-408 cyclohexyl H H n-butyl A-409 H CH₃ H n-butyl A-410 F CH₃ H n-butyl A-411 Cl CH₃ H n-butyl A-412 Br CH₃ H n-butyl A-413 CH₃ CH₃ H n-butyl A-414 CF₃ CH₃ H n-butyl A-415 OCH₃ CH₃ H n-butyl A-416 OCF₃ CH₃ H n-butyl A-417 cyclopropyl CH₃ H n-butyl A-418 cyclobutyl CH₃ H n-butyl A-419 cyclopentyl CH₃ H n-butyl A-420 cyclohexyl CH₃ H n-butyl A-421 H CH₃ CH₃ n-butyl A-422 F CH₃ CH₃ n-butyl A-423 Cl CH₃ CH₃ n-butyl A-424 Br CH₃ CH₃ n-butyl A-425 CH₃ CH₃ CH₃ n-butyl A-426 CF₃ CH₃ CH₃ n-butyl A-427 OCH₃ CH₃ CH₃ n-butyl A-428 OCF₃ CH₃ CH₃ n-butyl A-429 cyclopropyl CH₃ CH₃ n-butyl A-430 cyclobutyl CH₃ CH₃ n-butyl A-431 cyclopentyl CH₃ CH₃ n-butyl A-432 cyclohexyl CH₃ CH₃ n-butyl A-433 H H H cyclopropyl A-434 F H H cyclopropyl A-435 Cl H H cyclopropyl A-436 Br H H cyclopropyl A-437 CH₃ H H cyclopropyl A-438 CF₃ H H cyclopropyl A-439 OCH₃ H H cyclopropyl A-440 OCF₃ H H cyclopropyl A-441 cyclopropyl H H cyclopropyl A-442 cyclobutyl H H cyclopropyl A-443 cyclopentyl H H cyclopropyl A-444 cyclohexyl H H cyclopropyl A-445 H CH₃ H cyclopropyl A-446 F CH₃ H cyclopropyl A-447 Cl CH₃ H cyclopropyl A-448 Br CH₃ H cyclopropyl A-449 CH₃ CH₃ H cyclopropyl A-450 CF₃ CH₃ H cyclopropyl A-451 OCH₃ CH₃ H cyclopropyl A-452 OCF₃ CH₃ H cyclopropyl A-453 cyclopropyl CH₃ H cyclopropyl A-454 cyclobutyl CH₃ H cyclopropyl A-455 cyclopentyl CH₃ H cyclopropyl A-456 cyclohexyl CH₃ H cyclopropyl A-457 H CH₃ CH₃ cyclopropyl A-458 F CH₃ CH₃ cyclopropyl A-459 Cl CH₃ CH₃ cyclopropyl A-460 Br CH₃ CH₃ cyclopropyl A-461 CH₃ CH₃ CH₃ cyclopropyl A-462 CF₃ CH₃ CH₃ cyclopropyl A-463 OCH₃ CH₃ CH₃ cyclopropyl A-464 OCF₃ CH₃ CH₃ cyclopropyl A-465 cyclopropyl CH₃ CH₃ cyclopropyl A-466 cyclobutyl CH₃ CH₃ cyclopropyl A-467 cyclopentyl CH₃ CH₃ cyclopropyl A-468 cyclohexyl CH₃ CH₃ cyclopropyl A-469 H H H cyclobutyl A-470 F H H cyclobutyl A-471 Cl H H cyclobutyl A-472 Br H H cyclobutyl A-473 CH₃ H H cyclobutyl A-474 CF₃ H H cyclobutyl A-475 OCH₃ H H cyclobutyl A-476 OCF₃ H H cyclobutyl A-477 cyclopropyl H H cyclobutyl A-478 cyclobutyl H H cyclobutyl A-479 cyclopentyl H H cyclobutyl A-480 cyclohexyl H H cyclobutyl A-481 H CH₃ H cyclobutyl A-482 F CH₃ H cyclobutyl A-483 Cl CH₃ H cyclobutyl A-484 Br CH₃ H cyclobutyl A-485 CH₃ CH₃ H cyclobutyl A-486 CF₃ CH₃ H cyclobutyl A-487 OCH₃ CH₃ H cyclobutyl A-488 OCF₃ CH₃ H cyclobutyl A-489 cyclopropyl CH₃ H cyclobutyl A-490 cyclobutyl CH₃ H cyclobutyl A-491 cyclopentyl CH₃ H cyclobutyl A-492 cyclohexyl CH₃ H cyclobutyl A-493 H CH₃ CH₃ cyclobutyl A-494 F CH₃ CH₃ cyclobutyl A-495 Cl CH₃ CH₃ cyclobutyl A-496 Br CH₃ CH₃ cyclobutyl A-497 CH₃ CH₃ CH₃ cyclobutyl A-498 CF₃ CH₃ CH₃ cyclobutyl A-499 OCH₃ CH₃ CH₃ cyclobutyl A-500 OCF₃ CH₃ CH₃ cyclobutyl A-501 cyclopropyl CH₃ CH₃ cyclobutyl A-502 cyclobutyl CH₃ CH₃ cyclobutyl A-503 cyclopentyl CH₃ CH₃ cyclobutyl A-504 cyclohexyl CH₃ CH₃ cyclobutyl A-505 H H H cyclopentyl A-506 F H H cyclopentyl A-507 Cl H H cyclopentyl A-508 Br H H cyclopentyl A-509 CH₃ H H cyclopentyl A-510 CF₃ H H cyclopentyl A-511 OCH₃ H H cyclopentyl A-512 OCF₃ H H cyclopentyl A-513 cyclopropyl H H cyclopentyl A-514 cyclobutyl H H cyclopentyl A-515 cyclopentyl H H cyclopentyl A-516 cyclohexyl H H cyclopentyl A-517 H CH₃ H cyclopentyl A-518 F CH₃ H cyclopentyl A-519 Cl CH₃ H cyclopentyl A-520 Br CH₃ H cyclopentyl A-521 CH₃ CH₃ H cyclopentyl A-522 CF₃ CH₃ H cyclopentyl A-523 OCH₃ CH₃ H cyclopentyl A-524 OCF₃ CH₃ H cyclopentyl A-525 cyclopropyl CH₃ H cyclopentyl A-526 cyclobutyl CH₃ H cyclopentyl A-527 cyclopentyl CH₃ H cyclopentyl A-528 cyclohexyl CH₃ H cyclopentyl A-529 H CH₃ CH₃ cyclopentyl A-530 F CH₃ CH₃ cyclopentyl A-531 Cl CH₃ CH₃ cyclopentyl A-532 Br CH₃ CH₃ cyclopentyl A-533 CH₃ CH₃ CH₃ cyclopentyl A-534 CF₃ CH₃ CH₃ cyclopentyl A-535 OCH₃ CH₃ CH₃ cyclopentyl A-536 OCF₃ CH₃ CH₃ cyclopentyl A-537 cyclopropyl CH₃ CH₃ cyclopentyl A-538 cyclobutyl CH₃ CH₃ cyclopentyl A-539 cyclopentyl CH₃ CH₃ cyclopentyl A-540 cyclohexyl CH₃ CH₃ cyclopentyl A-541 H H H cyclohexyl A-542 F H H cyclohexyl A-543 Cl H H cyclohexyl A-544 Br H H cyclohexyl A-545 CH₃ H H cyclohexyl A-546 CF₃ H H cyclohexyl A-547 OCH₃ H H cyclohexyl A-548 OCF₃ H H cyclohexyl A-549 cyclopropyl H H cyclohexyl A-550 cyclobutyl H H cyclohexyl A-551 cyclopentyl H H cyclohexyl A-552 cyclohexyl H H cyclohexyl A-553 H CH₃ H cyclohexyl A-554 F CH₃ H cyclohexyl A-555 Cl CH₃ H cyclohexyl A-556 Br CH₃ H cyclohexyl A-557 CH₃ CH₃ H cyclohexyl A-558 CF₃ CH₃ H cyclohexyl A-559 OCH₃ CH₃ H cyclohexyl A-560 OCF₃ CH₃ H cyclohexyl A-561 cyclopropyl CH₃ H cyclohexyl A-562 cyclobutyl CH₃ H cyclohexyl A-563 cyclopentyl CH₃ H cyclohexyl A-564 cyclohexyl CH₃ H cyclohexyl A-565 H CH₃ CH₃ cyclohexyl A-566 F CH₃ CH₃ cyclohexyl A-567 Cl CH₃ CH₃ cyclohexyl A-568 Br CH₃ CH₃ cyclohexyl A-569 CH₃ CH₃ CH₃ cyclohexyl A-570 CF₃ CH₃ CH₃ cyclohexyl A-571 OCH₃ CH₃ CH₃ cyclohexyl A-572 OCF₃ CH₃ CH₃ cyclohexyl A-573 cyclopropyl CH₃ CH₃ cyclohexyl A-574 cyclobutyl CH₃ CH₃ cyclohexyl A-575 cyclopentyl CH₃ CH₃ cyclohexyl A-576 cyclohexyl CH₃ CH₃ cyclohexyl A-577 H H H oxetan-3-yl A-578 F H H oxetan-3-yl A-579 Cl H H oxetan-3-yl A-580 Br H H oxetan-3-yl A-581 CH₃ H H oxetan-3-yl A-582 CF₃ H H oxetan-3-yl A-583 OCH₃ H H oxetan-3-yl A-584 OCF₃ H H oxetan-3-yl A-585 cyclopropyl H H oxetan-3-yl A-586 cyclobutyl H H oxetan-3-yl A-587 cyclopentyl H H oxetan-3-yl A-588 cyclohexyl H H oxetan-3-yl A-589 H CH₃ H oxetan-3-yl A-590 F CH₃ H oxetan-3-yl A-591 Cl CH₃ H oxetan-3-yl A-592 Br CH₃ H oxetan-3-yl A-593 CH₃ CH₃ H oxetan-3-yl A-594 CF₃ CH₃ H oxetan-3-yl A-595 OCH₃ CH₃ H oxetan-3-yl A-596 OCF₃ CH₃ H oxetan-3-yl A-597 cyclopropyl CH₃ H oxetan-3-yl A-598 cyclobutyl CH₃ H oxetan-3-yl A-599 cyclopentyl CH₃ H oxetan-3-yl A-600 cyclohexyl CH₃ H oxetan-3-yl A-601 H CH₃ CH₃ oxetan-3-yl A-602 F CH₃ CH₃ oxetan-3-yl A-603 Cl CH₃ CH₃ oxetan-3-yl A-604 Br CH₃ CH₃ oxetan-3-yl A-605 CH₃ CH₃ CH₃ oxetan-3-yl A-606 CF₃ CH₃ CH₃ oxetan-3-yl A-607 OCH₃ CH₃ CH₃ oxetan-3-yl A-608 OCF₃ CH₃ CH₃ oxetan-3-yl A-609 cyclopropyl CH₃ CH₃ oxetan-3-yl A-610 cyclobutyl CH₃ CH₃ oxetan-3-yl A-611 cyclopentyl CH₃ CH₃ oxetan-3-yl A-612 cyclohexyl CH₃ CH₃ oxetan-3-yl A-613 H H H —CH₂-cyclopropyl A-614 F H H —CH₂-cyclopropyl A-615 Cl H H —CH₂-cyclopropyl A-616 Br H H —CH₂-cyclopropyl A-617 CH₃ H H —CH₂-cyclopropyl A-618 CF₃ H H —CH₂-cyclopropyl A-619 OCH₃ H H —CH₂-cyclopropyl A-620 OCF₃ H H —CH₂-cyclopropyl A-621 cyclopropyl H H —CH₂-cyclopropyl A-622 cyclobutyl H H —CH₂-cyclopropyl A-623 cyclopentyl H H —CH₂-cyclopropyl A-624 cyclohexyl H H —CH₂-cyclopropyl A-625 H CH₃ H —CH₂-cyclopropyl A-626 F CH₃ H —CH₂-cyclopropyl A-627 Cl CH₃ H —CH₂-cyclopropyl A-628 Br CH₃ H —CH₂-cyclopropyl A-629 CH₃ CH₃ H —CH₂-cyclopropyl A-630 CF₃ CH₃ H —CH₂-cyclopropyl A-631 OCH₃ CH₃ H —CH₂-cyclopropyl A-632 OCF₃ CH₃ H —CH₂-cyclopropyl A-633 cyclopropyl CH₃ H —CH₂-cyclopropyl A-634 cyclobutyl CH₃ H —CH₂-cyclopropyl A-635 cyclopentyl CH₃ H —CH₂-cyclopropyl A-636 cyclohexyl CH₃ H —CH₂-cyclopropyl A-637 H CH₃ CH₃ —CH₂-cyclopropyl A-638 F CH₃ CH₃ —CH₂-cyclopropyl A-639 Cl CH₃ CH₃ —CH₂-cyclopropyl A-640 Br CH₃ CH₃ —CH₂-cyclopropyl A-641 CH₃ CH₃ CH₃ —CH₂-cyclopropyl A-642 CF₃ CH₃ CH₃ —CH₂-cyclopropyl A-643 OCH₃ CH₃ CH₃ —CH₂-cyclopropyl A-644 OCF₃ CH₃ CH₃ —CH₂-cyclopropyl A-645 cyclopropyl CH₃ CH₃ —CH₂-cyclopropyl A-646 cyclobutyl CH₃ CH₃ —CH₂-cyclopropyl A-647 cyclopentyl CH₃ CH₃ —CH₂-cyclopropyl A-648 cyclohexyl CH₃ CH₃ —CH₂-cyclopropyl A-649 H H H —CH₂-cyclobutyl A-650 F H H —CH₂-cyclobutyl A-651 Cl H H —CH₂-cyclobutyl A-652 Br H H —CH₂-cyclobutyl A-653 CH₃ H H —CH₂-cyclobutyl A-654 CF₃ H H —CH₂-cyclobutyl A-655 OCH₃ H H —CH₂-cyclobutyl A-656 OCF₃ H H —CH₂-cyclobutyl A-657 cyclopropyl H H —CH₂-cyclobutyl A-658 cyclobutyl H H —CH₂-cyclobutyl A-659 cyclopentyl H H —CH₂-cyclobutyl A-660 cyclohexyl H H —CH₂-cyclobutyl A-661 H CH₃ H —CH₂-cyclobutyl A-662 F CH₃ H —CH₂-cyclobutyl A-663 Cl CH₃ H —CH₂-cyclobutyl A-664 Br CH₃ H —CH₂-cyclobutyl A-665 CH₃ CH₃ H —CH₂-cyclobutyl A-666 CF₃ CH₃ H —CH₂-cyclobutyl A-667 OCH₃ CH₃ H —CH₂-cyclobutyl A-668 OCF₃ CH₃ H —CH₂-cyclobutyl A-669 cyclopropyl CH₃ H —CH₂-cyclobutyl A-670 cyclobutyl CH₃ H —CH₂-cyclobutyl A-671 cyclopentyl CH₃ H —CH₂-cyclobutyl A-672 cyclohexyl CH₃ H —CH₂-cyclobutyl A-673 H CH₃ CH₃ —CH₂-cyclobutyl A-674 F CH₃ CH₃ —CH₂-cyclobutyl A-675 Cl CH₃ CH₃ —CH₂-cyclobutyl A-676 Br CH₃ CH₃ —CH₂-cyclobutyl A-677 CH₃ CH₃ CH₃ —CH₂-cyclobutyl A-678 CF₃ CH₃ CH₃ —CH₂-cyclobutyl A-679 OCH₃ CH₃ CH₃ —CH₂-cyclobutyl A-680 OCF₃ CH₃ CH₃ —CH₂-cyclobutyl A-681 cyclopropyl CH₃ CH₃ —CH₂-cyclobutyl A-682 cyclobutyl CH₃ CH₃ —CH₂-cyclobutyl A-683 cyclopentyl CH₃ CH₃ —CH₂-cyclobutyl A-684 cyclohexyl CH₃ CH₃ —CH₂-cyclobutyl A-685 H H H —CH₂-cyclopentyl A-686 F H H —CH₂-cyclopentyl A-687 Cl H H —CH₂-cyclopentyl A-688 Br H H —CH₂-cyclopentyl A-689 CH₃ H H —CH₂-cyclopentyl A-690 CF₃ H H —CH₂-cyclopentyl A-691 OCH₃ H H —CH₂-cyclopentyl A-692 OCF₃ H H —CH₂-cyclopentyl A-693 cyclopropyl H H —CH₂-cyclopentyl A-694 cyclobutyl H H —CH₂-cyclopentyl A-695 cyclopentyl H H —CH₂-cyclopentyl A-696 cyclohexyl H H —CH₂-cyclopentyl A-697 H CH₃ H —CH₂-cyclopentyl A-698 F CH₃ H —CH₂-cyclopentyl A-699 Cl CH₃ H —CH₂-cyclopentyl A-700 Br CH₃ H —CH₂-cyclopentyl A-701 CH₃ CH₃ H —CH₂-cyclopentyl A-702 CF₃ CH₃ H —CH₂-cyclopentyl A-703 OCH₃ CH₃ H —CH₂-cyclopentyl A-704 OCF₃ CH₃ H —CH₂-cyclopentyl A-705 cyclopropyl CH₃ H —CH₂-cyclopentyl A-706 cyclobutyl CH₃ H —CH₂-cyclopentyl A-707 cyclopentyl CH₃ H —CH₂-cyclopentyl A-708 cyclohexyl CH₃ H —CH₂-cyclopentyl A-709 H CH₃ CH₃ —CH₂-cyclopentyl A-710 F CH₃ CH₃ —CH₂-cyclopentyl A-711 Cl CH₃ CH₃ —CH₂-cyclopentyl A-712 Br CH₃ CH₃ —CH₂-cyclopentyl A-713 CH₃ CH₃ CH₃ —CH₂-cyclopentyl A-714 CF₃ CH₃ CH₃ —CH₂-cyclopentyl A-715 OCH₃ CH₃ CH₃ —CH₂-cyclopentyl A-716 OCF₃ CH₃ CH₃ —CH₂-cyclopentyl A-717 cyclopropyl CH₃ CH₃ —CH₂-cyclopentyl A-718 cyclobutyl CH₃ CH₃ —CH₂-cyclopentyl A-719 cyclopentyl CH₃ CH₃ —CH₂-cyclopentyl A-720 cyclohexyl CH₃ CH₃ —CH₂-cyclopentyl A-721 H H H —CH₂-cyclohexyl A-722 F H H —CH₂-cyclohexyl A-723 Cl H H —CH₂-cyclohexyl A-724 Br H H —CH₂-cyclohexyl A-725 CH₃ H H —CH₂-cyclohexyl A-726 CF₃ H H —CH₂-cyclohexyl A-727 OCH₃ H H —CH₂-cyclohexyl A-728 OCF₃ H H —CH₂-cyclohexyl A-729 cyclopropyl H H —CH₂-cyclohexyl A-730 cyclobutyl H H —CH₂-cyclohexyl A-731 cyclopentyl H H —CH₂-cyclohexyl A-732 cyclohexyl H H —CH₂-cyclohexyl A-733 H CH₃ H —CH₂-cyclohexyl A-734 F CH₃ H —CH₂-cyclohexyl A-735 Cl CH₃ H —CH₂-cyclohexyl A-736 Br CH₃ H —CH₂-cyclohexyl A-737 CH₃ CH₃ H —CH₂-cyclohexyl A-738 CF₃ CH₃ H —CH₂-cyclohexyl A-739 OCH₃ CH₃ H —CH₂-cyclohexyl A-740 OCF₃ CH₃ H —CH₂-cyclohexyl A-741 cyclopropyl CH₃ H —CH₂-cyclohexyl A-742 cyclobutyl CH₃ H —CH₂-cyclohexyl A-743 cyclopentyl CH₃ H —CH₂-cyclohexyl A-744 cyclohexyl CH₃ H —CH₂-cyclohexyl A-745 H CH₃ CH₃ —CH₂-cyclohexyl A-746 F CH₃ CH₃ —CH₂-cyclohexyl A-747 Cl CH₃ CH₃ —CH₂-cyclohexyl A-748 Br CH₃ CH₃ —CH₂-cyclohexyl A-749 CH₃ CH₃ CH₃ —CH₂-cyclohexyl A-750 CF₃ CH₃ CH₃ —CH₂-cyclohexyl A-751 OCH₃ CH₃ CH₃ —CH₂-cyclohexyl A-752 OCF₃ CH₃ CH₃ —CH₂-cyclohexyl A-753 cyclopropyl CH₃ CH₃ —CH₂-cyclohexyl A-754 cyclobutyl CH₃ CH₃ —CH₂-cyclohexyl A-755 cyclopentyl CH₃ CH₃ —CH₂-cyclohexyl A-756 cyclohexyl CH₃ CH₃ —CH₂-cyclohexyl A-757 H H H —C(O)-cyclopropyl A-758 F H H —C(O)-cyclopropyl A-759 Cl H H —C(O)-cyclopropyl A-760 Br H H —C(O)-cyclopropyl A-761 CH₃ H H —C(O)-cyclopropyl A-762 CF₃ H H —C(O)-cyclopropyl A-763 OCH₃ H H —C(O)-cyclopropyl A-764 OCF₃ H H —C(O)-cyclopropyl A-765 cyclopropyl H H —C(O)-cyclopropyl A-766 cyclobutyl H H —C(O)-cyclopropyl A-767 cyclopentyl H H —C(O)-cyclopropyl A-768 cyclohexyl H H —C(O)-cyclopropyl A-769 H CH₃ H —C(O)-cyclopropyl A-770 F CH₃ H —C(O)-cyclopropyl A-771 Cl CH₃ H —C(O)-cyclopropyl A-772 Br CH₃ H —C(O)-cyclopropyl A-773 CH₃ CH₃ H —C(O)-cyclopropyl A-774 CF₃ CH₃ H —C(O)-cyclopropyl A-775 OCH₃ CH₃ H —C(O)-cyclopropyl A-776 OCF₃ CH₃ H —C(O)-cyclopropyl A-777 cyclopropyl CH₃ H —C(O)-cyclopropyl A-778 cyclobutyl CH₃ H —C(O)-cyclopropyl A-779 cyclopentyl CH₃ H —C(O)-cyclopropyl A-780 cyclohexyl CH₃ H —C(O)-cyclopropyl A-781 H CH₃ CH₃ —C(O)-cyclopropyl A-782 F CH₃ CH₃ —C(O)-cyclopropyl A-783 Cl CH₃ CH₃ —C(O)-cyclopropyl A-784 Br CH₃ CH₃ —C(O)-cyclopropyl A-785 CH₃ CH₃ CH₃ —C(O)-cyclopropyl A-786 CF₃ CH₃ CH₃ —C(O)-cyclopropyl A-787 OCH₃ CH₃ CH₃ —C(O)-cyclopropyl A-788 OCF₃ CH₃ CH₃ —C(O)-cyclopropyl A-789 cyclopropyl CH₃ CH₃ —C(O)-cyclopropyl A-790 cyclobutyl CH₃ CH₃ —C(O)-cyclopropyl A-791 cyclopentyl CH₃ CH₃ —C(O)-cyclopropyl A-792 cyclohexyl CH₃ CH₃ —C(O)-cyclopropyl A-793 H H H —C(O)-cyclobutyl A-794 F H H —C(O)-cyclobutyl A-795 Cl H H —C(O)-cyclobutyl A-796 Br H H —C(O)-cyclobutyl A-797 CH₃ H H —C(O)-cyclobutyl A-798 CF₃ H H —C(O)-cyclobutyl A-799 OCH₃ H H —C(O)-cyclobutyl A-800 OCF₃ H H —C(O)-cyclobutyl A-801 cyclopropyl H H —C(O)-cyclobutyl A-802 cyclobutyl H H —C(O)-cyclobutyl A-803 cyclopentyl H H —C(O)-cyclobutyl A-804 cyclohexyl H H —C(O)-cyclobutyl A-805 H CH₃ H —C(O)-cyclobutyl A-806 F CH₃ H —C(O)-cyclobutyl A-807 Cl CH₃ H —C(O)-cyclobutyl A-808 Br CH₃ H —C(O)-cyclobutyl A-809 CH₃ CH₃ H —C(O)-cyclobutyl A-810 CF₃ CH₃ H —C(O)-cyclobutyl A-811 OCH₃ CH₃ H —C(O)-cyclobutyl A-812 OCF₃ CH₃ H —C(O)-cyclobutyl A-813 cyclopropyl CH₃ H —C(O)-cyclobutyl A-814 cyclobutyl CH₃ H —C(O)-cyclobutyl A-815 cyclopentyl CH₃ H —C(O)-cyclobutyl A-816 cyclohexyl CH₃ H —C(O)-cyclobutyl A-817 H CH₃ CH₃ —C(O)-cyclobutyl A-818 F CH₃ CH₃ —C(O)-cyclobutyl A-819 Cl CH₃ CH₃ —C(O)-cyclobutyl A-820 Br CH₃ CH₃ —C(O)-cyclobutyl A-821 CH₃ CH₃ CH₃ —C(O)-cyclobutyl A-822 CF₃ CH₃ CH₃ —C(O)-cyclobutyl A-823 OCH₃ CH₃ CH₃ —C(O)-cyclobutyl A-824 OCF₃ CH₃ CH₃ —C(O)-cyclobutyl A-825 cyclopropyl CH₃ CH₃ —C(O)-cyclobutyl A-826 cyclobutyl CH₃ CH₃ —C(O)-cyclobutyl A-827 cyclopentyl CH₃ CH₃ —C(O)-cyclobutyl A-828 cyclohexyl CH₃ CH₃ —C(O)-cyclobutyl A-829 H H H —C(O)-cyclopentyl A-830 F H H —C(O)-cyclopentyl A-831 Cl H H —C(O)-cyclopentyl A-832 Br H H —C(O)-cyclopentyl A-833 CH₃ H H —C(O)-cyclopentyl A-834 CF₃ H H —C(O)-cyclopentyl A-835 OCH₃ H H —C(O)-cyclopentyl A-836 OCF₃ H H —C(O)-cyclopentyl A-837 cyclopropyl H H —C(O)-cyclopentyl A-838 cyclobutyl H H —C(O)-cyclopentyl A-839 cyclopentyl H H —C(O)-cyclopentyl A-840 cyclohexyl H H —C(O)-cyclopentyl A-841 H CH₃ H —C(O)-cyclopentyl A-842 F CH₃ H —C(O)-cyclopentyl A-843 Cl CH₃ H —C(O)-cyclopentyl A-844 Br CH₃ H —C(O)-cyclopentyl A-845 CH₃ CH₃ H —C(O)-cyclopentyl A-846 CF₃ CH₃ H —C(O)-cyclopentyl A-847 OCH₃ CH₃ H —C(O)-cyclopentyl A-848 OCF₃ CH₃ H —C(O)-cyclopentyl A-849 cyclopropyl CH₃ H —C(O)-cyclopentyl A-850 cyclobutyl CH₃ H —C(O)-cyclopentyl A-851 cyclopentyl CH₃ H —C(O)-cyclopentyl A-852 cyclohexyl CH₃ H —C(O)-cyclopentyl A-853 H CH₃ CH₃ —C(O)-cyclopentyl A-854 F CH₃ CH₃ —C(O)-cyclopentyl A-855 Cl CH₃ CH₃ —C(O)-cyclopentyl A-856 Br CH₃ CH₃ —C(O)-cyclopentyl A-857 CH₃ CH₃ CH₃ —C(O)-cyclopentyl A-858 CF₃ CH₃ CH₃ —C(O)-cyclopentyl A-859 OCH₃ CH₃ CH₃ —C(O)-cyclopentyl A-860 OCF₃ CH₃ CH₃ —C(O)-cyclopentyl A-861 cyclopropyl CH₃ CH₃ —C(O)-cyclopentyl A-862 cyclobutyl CH₃ CH₃ —C(O)-cyclopentyl A-863 cyclopentyl CH₃ CH₃ —C(O)-cyclopentyl A-864 cyclohexyl CH₃ CH₃ —C(O)-cyclopentyl A-865 H H H —C(O)-cyclohexyl A-866 F H H —C(O)-cyclohexyl A-867 Cl H H —C(O)-cyclohexyl A-868 Br H H —C(O)-cyclohexyl A-869 CH₃ H H —C(O)-cyclohexyl A-870 CF₃ H H —C(O)-cyclohexyl A-871 OCH₃ H H —C(O)-cyclohexyl A-872 OCF₃ H H —C(O)-cyclohexyl A-873 cyclopropyl H H —C(O)-cyclohexyl A-874 cyclobutyl H H —C(O)-cyclohexyl A-875 cyclopentyl H H —C(O)-cyclohexyl A-876 cyclohexyl H H —C(O)-cyclohexyl A-877 H CH₃ H —C(O)-cyclohexyl A-878 F CH₃ H —C(O)-cyclohexyl A-879 Cl CH₃ H —C(O)-cyclohexyl A-880 Br CH₃ H —C(O)-cyclohexyl A-881 CH₃ CH₃ H —C(O)-cyclohexyl A-882 CF₃ CH₃ H —C(O)-cyclohexyl A-883 OCH₃ CH₃ H —C(O)-cyclohexyl A-884 OCF₃ CH₃ H —C(O)-cyclohexyl A-885 cyclopropyl CH₃ H —C(O)-cyclohexyl A-886 cyclobutyl CH₃ H —C(O)-cyclohexyl A-887 cyclopentyl CH₃ H —C(O)-cyclohexyl A-888 cyclohexyl CH₃ H —C(O)-cyclohexyl A-889 H CH₃ CH₃ —C(O)-cyclohexyl A-890 F CH₃ CH₃ —C(O)-cyclohexyl A-891 Cl CH₃ CH₃ —C(O)-cyclohexyl A-892 Br CH₃ CH₃ —C(O)-cyclohexyl A-893 CH₃ CH₃ CH₃ —C(O)-cyclohexyl A-894 CF₃ CH₃ CH₃ —C(O)-cyclohexyl A-895 OCH₃ CH₃ CH₃ —C(O)-cyclohexyl A-896 OCF₃ CH₃ CH₃ —C(O)-cyclohexyl A-897 cyclopropyl CH₃ CH₃ —C(O)-cyclohexyl A-898 cyclobutyl CH₃ CH₃ —C(O)-cyclohexyl A-899 cyclopentyl CH₃ CH₃ —C(O)-cyclohexyl A-900 cyclohexyl CH₃ CH₃ —C(O)-cyclohexyl A-901 H H —(CH₂)₃— A-902 F H —(CH₂)₃— A-903 Cl H —(CH₂)₃— A-904 Br H —(CH₂)₃— A-905 CH₃ H —(CH₂)₃— A-906 CF₃ H —(CH₂)₃— A-907 OCH₃ H —(CH₂)₃— A-908 OCF₃ H —(CH₂)₃— A-909 cyclopropyl H —(CH₂)₃— A-910 cyclobutyl H —(CH₂)₃— A-911 cyclopentyl H —(CH₂)₃— A-912 cyclohexyl H —(CH₂)₃— A-913 H CH₃ —(CH₂)₃— A-914 F CH₃ —(CH₂)₃— A-915 Cl CH₃ —(CH₂)₃— A-916 Br CH₃ —(CH₂)₃— A-917 CH₃ CH₃ —(CH₂)₃— A-918 CF₃ CH₃ —(CH₂)₃— A-919 OCH₃ CH₃ —(CH₂)₃— A-920 OCF₃ CH₃ —(CH₂)₃— A-921 cyclopropyl CH₃ —(CH₂)₃— A-922 cyclobutyl CH₃ —(CH₂)₃— A-923 cyclopentyl CH₃ —(CH₂)₃— A-924 cyclohexyl CH₃ —(CH₂)₃— A-925 H D —(CH₂)₃— A-926 F D —(CH₂)₃— A-927 Cl D —(CH₂)₃— A-928 Br D —(CH₂)₃— A-929 CH₃ D —(CH₂)₃— A-930 CF₃ D —(CH₂)₃— A-931 OCH₃ D —(CH₂)₃— A-932 OCF₃ D —(CH₂)₃— A-933 cyclopropyl D —(CH₂)₃— A-934 cyclobutyl D —(CH₂)₃— A-935 cyclopentyl D —(CH₂)₃— A-936 cyclohexyl D —(CH₂)₃— A-937 H H —(CH₂)₄— A-938 F H —(CH₂)₄— A-939 Cl H —(CH₂)₄— A-940 Br H —(CH₂)₄— A-941 CH₃ H —(CH₂)₄— A-942 CF₃ H —(CH₂)₄— A-943 OCH₃ H —(CH₂)₄— A-944 OCF₃ H —(CH₂)₄— A-945 cyclopropyl H —(CH₂)₄— A-946 cyclobutyl H —(CH₂)₄— A-947 cyclopentyl H —(CH₂)₄— A-948 cyclohexyl H —(CH₂)₄— A-949 H CH₃ —(CH₂)₄— A-950 F CH₃ —(CH₂)₄— A-951 Cl CH₃ —(CH₂)₄— A-952 Br CH₃ —(CH₂)₄— A-953 CH₃ CH₃ —(CH₂)₄— A-954 CF₃ CH₃ —(CH₂)₄— A-955 OCH₃ CH₃ —(CH₂)₄— A-956 OCF₃ CH₃ —(CH₂)₄— A-957 cyclopropyl CH₃ —(CH₂)₄— A-958 cyclobutyl CH₃ —(CH₂)₄— A-959 cyclopentyl CH₃ —(CH₂)₄— A-960 cyclohexyl CH₃ —(CH₂)₄— A-961 H D —(CH₂)₄— A-962 F D —(CH₂)₄— A-963 Cl D —(CH₂)₄— A-964 Br D —(CH₂)₄— A-965 CH₃ D —(CH₂)₄— A-966 CF₃ D —(CH₂)₄— A-967 OCH₃ D —(CH₂)₄— A-968 OCF₃ D —(CH₂)₄— A-969 cyclopropyl D —(CH₂)₄— A-970 cyclobutyl D —(CH₂)₄— A-971 cyclopentyl D —(CH₂)₄— A-972 cyclohexyl D —(CH₂)₄— A-973 H H —(CH₂)₅— A-974 F H —(CH₂)₅— A-975 Cl H —(CH₂)₅— A-976 Br H —(CH₂)₅— A-977 CH₃ H —(CH₂)₅— A-978 CF₃ H —(CH₂)₅— A-979 OCH₃ H —(CH₂)₅— A-980 OCF₃ H —(CH₂)₅— A-981 cyclopropyl H —(CH₂)₅— A-982 cyclobutyl H —(CH₂)₅— A-983 cyclopentyl H —(CH₂)₅— A-984 cyclohexyl H —(CH₂)₅— A-985 H CH₃ —(CH₂)₅— A-986 F CH₃ —(CH₂)₅— A-987 Cl CH₃ —(CH₂)₅— A-988 Br CH₃ —(CH₂)₅— A-989 CH₃ CH₃ —(CH₂)₅— A-990 CF₃ CH₃ —(CH₂)₅— A-991 OCH₃ CH₃ —(CH₂)₅— A-992 OCF₃ CH₃ —(CH₂)₅— A-993 cyclopropyl CH₃ —(CH₂)₅— A-994 cyclobutyl CH₃ —(CH₂)₅— A-995 cyclopentyl CH₃ —(CH₂)₅— A-996 cyclohexyl CH₃ —(CH₂)₅— A-997 H D —(CH₂)₅— A-998 F D —(CH₂)₅— A-999 Cl D —(CH₂)₅— A-1000 Br D —(CH₂)₅— A-1001 CH₃ D —(CH₂)₅— A-1002 CF₃ D —(CH₂)₅— A-1003 OCH₃ D —(CH₂)₅— A-1004 OCF₃ D —(CH₂)₅— A-1005 cyclopropyl D —(CH₂)₅— A-1006 cyclobutyl D —(CH₂)₅— A-1007 cyclopentyl D —(CH₂)₅— A-1008 cyclohexyl D —(CH₂)₅— A-1009 F H —(CH₂—CH-(μ-CH₂)—CH)—*** A-1010 Cl H —(CH₂—CH-(μ-CH₂)—CH)— A-1011 Br H —(CH₂—CH-(μ-CH₂)—CH)— A-1012 CH₃ H —(CH₂—CH-(μ-CH₂)—CH)— A-1013 CF₃ H —(CH₂—CH-(μ-CH₂)—CH)— A-1014 OCH₃ H —(CH₂—CH-(μ-CH₂)—CH)— A-1015 OCF₃ H —(CH₂—CH-(μ-CH₂)—CH)— A-1016 cyclopropyl H —(CH₂—CH-(μ-CH₂)—CH)— A-1017 cyclobutyl H —(CH₂—CH-(μ-CH₂)—CH)— A-1018 cyclopentyl H —(CH₂—CH-(μ-CH₂)—CH)— A-1019 cyclohexyl H —(CH₂—CH-(μ-CH₂)—CH)— A-1020 H CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1021 F CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1022 Cl CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1023 Br CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1024 CH₃ CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1025 CF₃ CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1026 OCH₃ CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1027 OCF₃ CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1028 cyclopropyl CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1029 cyclobutyl CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1030 cyclopentyl CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1031 cyclohexyl CH₃ —(CH₂—CH-(μ-CH₂)—CH)— A-1032 H D —(CH₂—CH-(μ-CH₂)—CH)— A-1033 F D —(CH₂—CH-(μ-CH₂)—CH)— A-1034 Cl D —(CH₂—CH-(μ-CH₂)—CH)— A-1035 Br D —(CH₂—CH-(μ-CH₂)—CH)— A-1036 CH₃ D —(CH₂—CH-(μ-CH₂)—CH)— A-1037 CF₃ D —(CH₂—CH-(μ-CH₂)—CH)— A-1038 OCH₃ D —(CH₂—CH-(μ-CH₂)—CH)— A-1039 OCF₃ D —(CH₂—CH-(μ-CH₂)—CH)— A-1040 cyclopropyl D —(CH₂—CH-(μ-CH₂)—CH)— A-1041 cyclobutyl D —(CH₂—CH-(μ-CH₂)—CH)— A-1042 cyclopentyl D —(CH₂—CH-(μ-CH₂)—CH)— A-1043 cyclohexyl D —(CH₂—CH-(μ-CH₂)—CH)— *C₆H₅ = phenyl **C₆H₄CH₃ = 4-methylphenyl (p-tolyl) ***—(CH₂—CH-(μ-CH₂)—CH)— =

(# = attachment point to the atoms carrying R⁶ (left #) and R^(5a) (right #))

TABLE B No. R^(9a) R^(5b) R^(5a) R⁷ R⁸ B-1 H H H CH₃ CH₃ B-2 F H H CH₃ CH₃ B-3 Cl H H CH₃ CH₃ B-4 Br H H CH₃ CH₃ B-5 CH₃ H H CH₃ CH₃ B-6 CF₃ H H CH₃ CH₃ B-7 OCH₃ H H CH₃ CH₃ B-8 OCF₃ H H CH₃ CH₃ B-9 H F H CH₃ CH₃ B-10 F F H CH₃ CH₃ B-11 Cl F H CH₃ CH₃ B-12 Br F H CH₃ CH₃ B-13 CH₃ F H CH₃ CH₃ B-14 CF₃ F H CH₃ CH₃ B-15 OCH₃ F H CH₃ CH₃ B-16 OCF₃ F H CH₃ CH₃ B-17 H Cl H CH₃ CH₃ B-18 F Cl H CH₃ CH₃ B-19 Cl Cl H CH₃ CH₃ B-20 Br Cl H CH₃ CH₃ B-21 CH₃ Cl H CH₃ CH₃ B-22 CF₃ Cl H CH₃ CH₃ B-23 OCH₃ Cl H CH₃ CH₃ B-24 OCF₃ Cl H CH₃ CH₃ B-25 H CH₃ H CH₃ CH₃ B-26 F CH₃ H CH₃ CH₃ B-27 Cl CH₃ H CH₃ CH₃ B-28 Br CH₃ H CH₃ CH₃ B-29 CH₃ CH₃ H CH₃ CH₃ B-30 CF₃ CH₃ H CH₃ CH₃ B-31 OCH₃ CH₃ H CH₃ CH₃ B-32 OCF₃ CH₃ H CH₃ CH₃ B-33 H CH₃ CH₃ CH₃ CH₃ B-34 F CH₃ CH₃ CH₃ CH₃ B-35 Cl CH₃ CH₃ CH₃ CH₃ B-36 Br CH₃ CH₃ CH₃ CH₃ B-37 CH₃ CH₃ CH₃ CH₃ CH₃ B-38 CF₃ CH₃ CH₃ CH₃ CH₃ B-39 OCH₃ CH₃ CH₃ CH₃ CH₃ B-40 OCF₃ CH₃ CH₃ CH₃ CH₃ B-41 H H H CH₃ CH₂CH₃ B-42 F H H CH₃ CH₂CH₃ B-43 Cl H H CH₃ CH₂CH₃ B-44 Br H H CH₃ CH₂CH₃ B-45 CH₃ H H CH₃ CH₂CH₃ B-46 CF₃ H H CH₃ CH₂CH₃ B-47 OCH₃ H H CH₃ CH₂CH₃ B-48 OCF₃ H H CH₃ CH₂CH₃ B-49 H F H CH₃ CH₂CH₃ B-50 F F H CH₃ CH₂CH₃ B-51 Cl F H CH₃ CH₂CH₃ B-52 Br F H CH₃ CH₂CH₃ B-53 CH₃ F H CH₃ CH₂CH₃ B-54 CF₃ F H CH₃ CH₂CH₃ B-55 OCH₃ F H CH₃ CH₂CH₃ B-56 OCF₃ F H CH₃ CH₂CH₃ B-57 H Cl H CH₃ CH₂CH₃ B-58 F Cl H CH₃ CH₂CH₃ B-59 Cl Cl H CH₃ CH₂CH₃ B-60 Br Cl H CH₃ CH₂CH₃ B-61 CH₃ Cl H CH₃ CH₂CH₃ B-62 CF₃ Cl H CH₃ CH₂CH₃ B-63 OCH₃ Cl H CH₃ CH₂CH₃ B-64 OCF₃ Cl H CH₃ CH₂CH₃ B-65 H CH₃ H CH₃ CH₂CH₃ B-66 F CH₃ H CH₃ CH₂CH₃ B-67 Cl CH₃ H CH₃ CH₂CH₃ B-68 Br CH₃ H CH₃ CH₂CH₃ B-69 CH₃ CH₃ H CH₃ CH₂CH₃ B-70 CF₃ CH₃ H CH₃ CH₂CH₃ B-71 OCH₃ CH₃ H CH₃ CH₂CH₃ B-72 OCF₃ CH₃ H CH₃ CH₂CH₃ B-73 H CH₃ CH₃ CH₃ CH₂CH₃ B-74 F CH₃ CH₃ CH₃ CH₂CH₃ B-75 Cl CH₃ CH₃ CH₃ CH₂CH₃ B-76 Br CH₃ CH₃ CH₃ CH₂CH₃ B-77 CH₃ CH₃ CH₃ CH₃ CH₂CH₃ B-78 CF₃ CH₃ CH₃ CH₃ CH₂CH₃ B-79 OCH₃ CH₃ CH₃ CH₃ CH₂CH₃ B-80 OCF₃ CH₃ CH₃ CH₃ CH₂CH₃ B-81 H H H CH₃ CF₃ B-82 F H H CH₃ CF₃ B-83 Cl H H CH₃ CF₃ B-84 Br H H CH₃ CF₃ B-85 CH₃ H H CH₃ CF₃ B-86 CF₃ H H CH₃ CF₃ B-87 OCH₃ H H CH₃ CF₃ B-88 OCF₃ H H CH₃ CF₃ B-89 H F H CH₃ CF₃ B-90 F F H CH₃ CF₃ B-91 Cl F H CH₃ CF₃ B-92 Br F H CH₃ CF₃ B-93 CH₃ F H CH₃ CF₃ B-94 CF₃ F H CH₃ CF₃ B-95 OCH₃ F H CH₃ CF₃ B-96 OCF₃ F H CH₃ CF₃ B-97 H Cl H CH₃ CF₃ B-98 F Cl H CH₃ CF₃ B-99 Cl Cl H CH₃ CF₃ B-100 Br Cl H CH₃ CF₃ B-101 CH₃ Cl H CH₃ CF₃ B-102 CF₃ Cl H CH₃ CF₃ B-103 OCH₃ Cl H CH₃ CF₃ B-104 OCF₃ Cl H CH₃ CF₃ B-105 H CH₃ H CH₃ CF₃ B-106 F CH₃ H CH₃ CF₃ B-107 Cl CH₃ H CH₃ CF₃ B-108 Br CH₃ H CH₃ CF₃ B-109 CH₃ CH₃ H CH₃ CF₃ B-110 CF₃ CH₃ H CH₃ CF₃ B-111 OCH₃ CH₃ H CH₃ CF₃ B-112 OCF₃ CH₃ H CH₃ CF₃ B-113 H CH₃ CH₃ CH₃ CF₃ B-114 F CH₃ CH₃ CH₃ CF₃ B-115 Cl CH₃ CH₃ CH₃ CF₃ B-116 Br CH₃ CH₃ CH₃ CF₃ B-117 CH₃ CH₃ CH₃ CH₃ CF₃ B-118 CF₃ CH₃ CH₃ CH₃ CF₃ B-119 OCH₃ CH₃ CH₃ CH₃ CF₃ B-120 OCF₃ CH₃ CH₃ CH₃ CF₃ B-121 H H H CF₃ CF₃ B-122 F H H CF₃ CF₃ B-123 Cl H H CF₃ CF₃ B-124 Br H H CF₃ CF₃ B-125 CH₃ H H CF₃ CF₃ B-126 CF₃ H H CF₃ CF₃ B-127 OCH₃ H H CF₃ CF₃ B-128 OCF₃ H H CF₃ CF₃ B-129 H F H CF₃ CF₃ B-130 F F H CF₃ CF₃ B-131 Cl F H CF₃ CF₃ B-132 Br F H CF₃ CF₃ B-133 CH₃ F H CF₃ CF₃ B-134 CF₃ F H CF₃ CF₃ B-135 OCH₃ F H CF₃ CF₃ B-136 OCF₃ F H CF₃ CF₃ B-137 H Cl H CF₃ CF₃ B-138 F Cl H CF₃ CF₃ B-139 Cl Cl H CF₃ CF₃ B-140 Br Cl H CF₃ CF₃ B-141 CH₃ Cl H CF₃ CF₃ B-142 CF₃ Cl H CF₃ CF₃ B-143 OCH₃ Cl H CF₃ CF₃ B-144 OCF₃ Cl H CF₃ CF₃ B-145 H CH₃ H CF₃ CF₃ B-146 F CH₃ H CF₃ CF₃ B-147 Cl CH₃ H CF₃ CF₃ B-148 Br CH₃ H CF₃ CF₃ B-149 CH₃ CH₃ H CF₃ CF₃ B-150 CF₃ CH₃ H CF₃ CF₃ B-151 OCH₃ CH₃ H CF₃ CF₃ B-152 OCF₃ CH₃ H CF₃ CF₃ B-153 H CH₃ CH₃ CF₃ CF₃ B-154 F CH₃ CH₃ CF₃ CF₃ B-155 Cl CH₃ CH₃ CF₃ CF₃ B-156 Br CH₃ CH₃ CF₃ CF₃ B-157 CH₃ CH₃ CH₃ CF₃ CF₃ B-158 CF₃ CH₃ CH₃ CF₃ CF₃ B-159 OCH₃ CH₃ CH₃ CF₃ CF₃ B-160 OCF₃ CH₃ CH₃ CF₃ CF₃ B-161 H H H CH₃ C₆H₅* B-162 F H H CH₃ C₆H₅ B-163 Cl H H CH₃ C₆H₅ B-164 Br H H CH₃ C₆H₅ B-165 CH₃ H H CH₃ C₆H₅ B-166 CF₃ H H CH₃ C₆H₅ B-167 OCH₃ H H CH₃ C₆H₅ B-168 OCF₃ H H CH₃ C₆H₅ B-169 H F H CH₃ C₆H₅ B-170 F F H CH₃ C₆H₅ B-171 Cl F H CH₃ C₆H₅ B-172 Br F H CH₃ C₆H₅ B-173 CH₃ F H CH₃ C₆H₅ B-174 CF₃ F H CH₃ C₆H₅ B-175 OCH₃ F H CH₃ C₆H₅ B-176 OCF₃ F H CH₃ C₆H₅ B-177 H Cl H CH₃ C₆H₅ B-178 F Cl H CH₃ C₆H₅ B-179 Cl Cl H CH₃ C₆H₅ B-180 Br Cl H CH₃ C₆H₅ B-181 CH₃ Cl H CH₃ C₆H₅ B-182 CF₃ Cl H CH₃ C₆H₅ B-183 OCH₃ Cl H CH₃ C₆H₅ B-184 OCF₃ Cl H CH₃ C₆H₅ B-185 H CH₃ H CH₃ C₆H₅ B-186 F CH₃ H CH₃ C₆H₅ B-187 Cl CH₃ H CH₃ C₆H₅ B-188 Br CH₃ H CH₃ C₆H₅ B-189 CH₃ CH₃ H CH₃ C₆H₅ B-190 CF₃ CH₃ H CH₃ C₆H₅ B-191 OCH₃ CH₃ H CH₃ C₆H₅ B-192 OCF₃ CH₃ H CH₃ C₆H₅ B-193 H CH₃ CH₃ CH₃ C₆H₅ B-194 F CH₃ CH₃ CH₃ C₆H₅ B-195 Cl CH₃ CH₃ CH₃ C₆H₅ B-196 Br CH₃ CH₃ CH₃ C₆H₅ B-197 CH₃ CH₃ CH₃ CH₃ C₆H₅ B-198 CF₃ CH₃ CH₃ CH₃ C₆H₅ B-199 OCH₃ CH₃ CH₃ CH₃ C₆H₅ B-200 OCF₃ CH₃ CH₃ CH₃ C₆H₅ B-201 H H H CH₃ OCH₃ B-202 F H H CH₃ OCH₃ B-203 Cl H H CH₃ OCH₃ B-204 Br H H CH₃ OCH₃ B-205 CH₃ H H CH₃ OCH₃ B-206 CF₃ H H CH₃ OCH₃ B-207 OCH₃ H H CH₃ OCH₃ B-208 OCF₃ H H CH₃ OCH₃ B-209 H F H CH₃ OCH₃ B-210 F F H CH₃ OCH₃ B-211 Cl F H CH₃ OCH₃ B-212 Br F H CH₃ OCH₃ B-213 CH₃ F H CH₃ OCH₃ B-214 CF₃ F H CH₃ OCH₃ B-215 OCH₃ F H CH₃ OCH₃ B-216 OCF₃ F H CH₃ OCH₃ B-217 H Cl H CH₃ OCH₃ B-218 F Cl H CH₃ OCH₃ B-219 Cl Cl H CH₃ OCH₃ B-220 Br Cl H CH₃ OCH₃ B-221 CH₃ Cl H CH₃ OCH₃ B-222 CF₃ Cl H CH₃ OCH₃ B-223 OCH₃ Cl H CH₃ OCH₃ B-224 OCF₃ Cl H CH₃ OCH₃ B-225 H CH₃ H CH₃ OCH₃ B-226 F CH₃ H CH₃ OCH₃ B-227 Cl CH₃ H CH₃ OCH₃ B-228 Br CH₃ H CH₃ OCH₃ B-229 CH₃ CH₃ H CH₃ OCH₃ B-230 CF₃ CH₃ H CH₃ OCH₃ B-231 OCH₃ CH₃ H CH₃ OCH₃ B-232 OCH₃ CH₃ H CH₃ OCH₃ B-233 H CH₃ CH₃ CH₃ OCH₃ B-234 F CH₃ CH₃ CH₃ OCH₃ B-235 Cl CH₃ CH₃ CH₃ OCH₃ B-236 Br CH₃ CH₃ CH₃ OCH₃ B-237 CH₃ CH₃ CH₃ CH₃ OCH₃ B-238 CF₃ CH₃ CH₃ CH₃ OCH₃ B-239 OCH₃ CH₃ CH₃ CH₃ OCH₃ B-240 OCF₃ CH₃ CH₃ CH₃ OCH₃ B-241 H H H CH₃ OH B-242 Fv H H CH₃ OH B-243 Cl H H CH₃ OH B-244 Br H H CH₃ OH B-245 CH₃ H H CH₃ OH B-246 CF₃ H H CH₃ OH B-247 OCH₃ H H CH₃ OH B-248 OCF₃ H H CH₃ OH B-249 H F H CH₃ OH B-250 F F H CH₃ OH B-251 Cl F H CH₃ OH B-252 Br F H CH₃ OH B-253 CH₃ F H CH₃ OH B-254 CF₃ F H CH₃ OH B-255 OCH₃ F H CH₃ OH B-256 OCF₃ F H CH₃ OH B-257 H Cl H CH₃ OH B-258 F Cl H CH₃ OH B-259 Cl Cl H CH₃ OH B-260 Br Cl H CH₃ OH B-261 CH₃ Cl H CH₃ OH B-262 CF₃ Cl H CH₃ OH B-263 OCH₃ Cl H CH₃ OH B-264 OCF₃ Cl H CH₃ OH B-265 H CH₃ H CH₃ OH B-266 F CH₃ H CH₃ OH B-267 Cl CH₃ H CH₃ OH B-268 Br CH₃ H CH₃ OH B-269 CH₃ CH₃ H CH₃ OH B-270 CF₃ CH₃ H CH₃ OH B-271 OCH₃ CH₃ H CH₃ OH B-272 OCF₃ CH₃ H CH₃ OH B-273 H CH₃ CH₃ CH₃ OH B-274 F CH₃ CH₃ CH₃ OH B-275 Cl CH₃ CH₃ CH₃ OH B-276 Br CH₃ CH₃ CH₃ OH B-277 CH₃ CH₃ CH₃ CH₃ OH B-278 CF₃ CH₃ CH₃ CH₃ OH B-279 OCH₃ CH₃ CH₃ CH₃ OH B-280 OCF₃ CH₃ CH₃ CH₃ OH B-281 H H H —(CH₂)₂— B-282 F H H —(CH₂)₂— B-283 Cl H H —(CH₂)₂— B-284 Br H H —(CH₂)₂— B-285 CH₃ H H —(CH₂)₂— B-286 CF₃ H H —(CH₂)₂— B-287 OCH₃ H H —(CH₂)₂— B-288 OCF₃ H H —(CH₂)₂— B-289 H F H —(CH₂)₂— B-290 F F H —(CH₂)₂— B-291 Cl F H —(CH₂)₂— B-292 Br F H —(CH₂)₂— B-293 CH₃ F H —(CH₂)₂— B-294 CF₃ F H —(CH₂)₂— B-295 OCH₃ F H —(CH₂)₂— B-296 OCF₃ F H —(CH₂)₂— B-297 H Cl H —(CH₂)₂— B-298 F Cl H —(CH₂)₂— B-299 Cl Cl H —(CH₂)₂— B-300 Br Cl H —(CH₂)₂— B-301 CH₃ Cl H —(CH₂)₂— B-302 CF₃ Cl H —(CH₂)₂— B-303 OCH₃ Cl H —(CH₂)₂— B-304 OCF₃ Cl H —(CH₂)₂— B-305 H CH₃ H —(CH₂)₂— B-306 F CH₃ H —(CH₂)₂— B-307 Cl CH₃ H —(CH₂)₂— B-308 Br CH₃ H —(CH₂)₂— B-309 CH₃ CH₃ H —(CH₂)₂— B-310 CF₃ CH₃ H —(CH₂)₂— B-311 OCH₃ CH₃ H —(CH₂)₂— B-312 OCF₃ CH₃ H —(CH₂)₂— B-313 H CH₃ CH₃ —(CH₂)₂— B-314 F CH₃ CH₃ —(CH₂)₂— B-315 Cl CH₃ CH₃ —(CH₂)₂— B-316 Br CH₃ CH₃ —(CH₂)₂— B-317 CH₃ CH₃ CH₃ —(CH₂)₂— B-318 CF₃ CH₃ CH₃ —(CH₂)₂— B-319 OCH₃ CH₃ CH₃ —(CH₂)₂— B-320 OCF₃ CH₃ CH₃ —(CH₂)₂— B-321 H H H —(CH₂)₃— B-322 F H H —(CH₂)₃— B-323 Cl H H —(CH₂)₃— B-324 Br H H —(CH₂)₃— B-325 CH₃ H H —(CH₂)₃— B-326 CF₃ H H —(CH₂)₃— B-327 OCH₃ H H —(CH₂)₃— B-328 OCF₃ H H —(CH₂)₃— B-329 H F H —(CH₂)₃— B-330 F F H —(CH₂)₃— B-331 Cl F H —(CH₂)₃— B-332 Br F H —(CH₂)₃— B-333 CH₃ F H —(CH₂)₃— B-334 CF₃ F H —(CH₂)₃— B-335 OCH₃ F H —(CH₂)₃— B-336 OCF₃ F H —(CH₂)₃— B-337 H Cl H —(CH₂)₃— B-338 F Cl H —(CH₂)₃— B-339 Cl Cl H —(CH₂)₃— B-340 Br Cl H —(CH₂)₃— B-341 CH₃ Cl H —(CH₂)₃— B-342 CF₃ Cl H —(CH₂)₃— B-343 OCH₃ Cl H —(CH₂)₃— B-344 OCF₃ Cl H —(CH₂)₃— B-345 H CH₃ H —(CH₂)₃— B-346 F CH₃ H —(CH₂)₃— B-347 Cl CH₃ H —(CH₂)₃— B-348 Br CH₃ H —(CH₂)₃— B-349 CH₃ CH₃ H —(CH₂)₃— B-350 CF₃ CH₃ H —(CH₂)₃— B-351 OCH₃ CH₃ H —(CH₂)₃— B-352 OCF₃ CH₃ H —(CH₂)₃— B-353 H CH₃ CH₃ —(CH₂)₃— B-354 F CH₃ CH₃ —(CH₂)₃— B-355 Cl CH₃ CH₃ —(CH₂)₃— B-356 Br CH₃ CH₃ —(CH₂)₃— B-357 CH₃ CH₃ CH₃ —(CH₂)₃— B-358 CF₃ CH₃ CH₃ —(CH₂)₃— B-359 OCH₃ CH₃ CH₃ —(CH₂)₃— B-360 OCF₃ CH₃ CH₃ —(CH₂)₃— B-361 H H H —(CH₂)₄— B-362 F H H —(CH₂)₄— B-363 Cl H H —(CH₂)₄— B-364 Br H H —(CH₂)₄— B-365 CH₃ H H —(CH₂)₄— B-366 CF₃ H H —(CH₂)₄— B-367 OCH₃ H H —(CH₂)₄— B-368 OCF₃ H H —(CH₂)₄— B-369 H F H —(CH₂)₄— B-370 F F H —(CH₂)₄— B-371 Cl F H —(CH₂)₄— B-372 Br F H —(CH₂)₄— B-373 CH₃ F H —(CH₂)₄— B-374 CF₃ F H —(CH₂)₄— B-375 OCH₃ F H —(CH₂)₄— B-376 OCF₃ F H —(CH₂)₄— B-377 H Cl H —(CH₂)₄— B-378 F Cl H —(CH₂)₄— B-379 Cl Cl H —(CH₂)₄— B-380 Br Cl H —(CH₂)₄— B-381 CH₃ Cl H —(CH₂)₄— B-382 CF₃ Cl H —(CH₂)₄— B-383 OCH₃ Cl H —(CH₂)₄— B-384 OCF₃ Cl H —(CH₂)₄— B-385 H CH₃ H —(CH₂)₄— B-386 F CH₃ H —(CH₂)₄— B-387 Cl CH₃ H —(CH₂)₄— B-388 Br CH₃ H —(CH₂)₄— B-389 CH₃ CH₃ H —(CH₂)₄— B-390 CF₃ CH₃ H —(CH₂)₄— B-391 OCH₃ CH₃ H —(CH₂)₄— B-392 OCF₃ CH₃ H —(CH₂)₄— B-393 H CH₃ CH₃ —(CH₂)₄— B-394 F CH₃ CH₃ —(CH₂)₄— B-395 Cl CH₃ CH₃ —(CH₂)₄— B-396 Br CH₃ CH₃ —(CH₂)₄— B-397 CH₃ CH₃ CH₃ —(CH₂)₄— B-398 CF₃ CH₃ CH₃ —(CH₂)₄— B-399 OCH₃ CH₃ CH₃ —(CH₂)₄— B-400 OCF₃ CH₃ CH₃ —(CH₂)₄— B-401 H H H —(CH₂)₅— B-402 F H H —(CH₂)₅— B-403 Cl H H —(CH₂)₅— B-404 Br H H —(CH₂)₅— B-405 CH₃ H H —(CH₂)₅— B-406 CF₃ H H —(CH₂)₅— B-407 OCH₃ H H —(CH₂)₅— B-408 OCF₃ H H —(CH₂)₅— B-409 H F H —(CH₂)₅— B-410 F F H —(CH₂)₅— B-411 Cl F H —(CH₂)₅— B-412 Br F H —(CH₂)₅— B-413 CH₃ F H —(CH₂)₅— B-414 CF₃ F H —(CH₂)₅— B-415 OCH₃ F H —(CH₂)₅— B-416 OCF₃ F H —(CH₂)₅— B-417 H Cl H —(CH₂)₅— B-418 F Cl H —(CH₂)₅— B-419 Cl Cl H —(CH₂)₅— B-420 Br Cl H —(CH₂)₅— B-421 CH₃ Cl H —(CH₂)₅— B-422 CF₃ Cl H —(CH₂)₅— B-423 OCH₃ Cl H —(CH₂)₅— B-424 OCF₃ Cl H —(CH₂)₅— B-425 H CH₃ H —(CH₂)₅— B-426 F CH₃ H —(CH₂)₅— B-427 Cl CH₃ H —(CH₂)₅— B-428 Br CH₃ H —(CH₂)₅— B-429 CH₃ CH₃ H —(CH₂)₅— B-430 CF₃ CH₃ H —(CH₂)₅— B-431 OCH₃ CH₃ H —(CH₂)₅— B-432 OCF₃ CH₃ H —(CH₂)₅— B-433 H CH₃ CH₃ —(CH₂)₅— B-434 F CH₃ CH₃ —(CH₂)₅— B-435 Cl CH₃ CH₃ —(CH₂)₅— B-436 Br CH₃ CH₃ —(CH₂)₅— B-437 CH₃ CH₃ CH₃ —(CH₂)₅— B-438 CF₃ CH₃ CH₃ —(CH₂)₅— B-439 OCH₃ CH₃ CH₃ —(CH₂)₅— B-440 OCF₃ CH₃ CH₃ —(CH₂)₅— B-441 H H H —(CH₂)₆— B-442 F H H —(CH₂)₆— B-443 Cl H H —(CH₂)₆— B-444 Br H H —(CH₂)₆— B-445 CH₃ H H —(CH₂)₆— B-446 CF₃ H H —(CH₂)₆— B-447 OCH₃ H H —(CH₂)₆— B-448 OCF₃ H H —(CH₂)₆— B-449 H F H —(CH₂)₆— B-450 F F H —(CH₂)₆— B-451 Cl F H —(CH₂)₆— B-452 Br F H —(CH₂)₆— B-453 CH₃ F H —(CH₂)₆— B-454 CF₃ F H —(CH₂)₆— B-455 OCH₃ F H —(CH₂)₆— B-456 OCF₃ F H —(CH₂)₆— B-457 H Cl H —(CH₂)₆— B-458 F Cl H —(CH₂)₆— B-459 Cl Cl H —(CH₂)₆— B-460 Br Cl H —(CH₂)₆— B-461 CH₃ Cl H —(CH₂)₆— B-462 CF₃ Cl H —(CH₂)₆— B-463 OCH₃ Cl H —(CH₂)₆— B-464 OCF₃ Cl H —(CH₂)₆— B-465 H CH₃ H —(CH₂)₆— B-466 F CH₃ H —(CH₂)₆— B-467 Cl CH₃ H —(CH₂)₆— B-468 Br CH₃ H —(CH₂)₆— B-469 CH₃ CH₃ H —(CH₂)₆— B-470 CF₃ CH₃ H —(CH₂)₆— B-471 OCH₃ CH₃ H —(CH₂)₆— B-472 OCF₃ CH₃ H —(CH₂)₆— B-473 H CH₃ CH₃ —(CH₂)₆— B-474 F CH₃ CH₃ —(CH₂)₆— B-475 Cl CH₃ CH₃ —(CH₂)₆— B-476 Br CH₃ CH₃ —(CH₂)₆— B-477 CH₃ CH₃ CH₃ —(CH₂)₆— B-478 CF₃ CH₃ CH₃ —(CH₂)₆— B-479 OCH₃ CH₃ CH₃ —(CH₂)₆— B-480 OCF₃ CH₃ CH₃ —(CH₂)₆— B-481 H H H —CH═CH—CH₂—CH₂— B-482 F H H —CH═CH—CH₂—CH₂— B-483 Cl H H —CH═CH—CH₂—CH₂— B-484 Br H H —CH═CH—CH₂—CH₂— B-485 CH₃ H H —CH═CH—CH₂—CH₂— B-486 CF₃ H H —CH═CH—CH₂—CH₂— B-487 OCH₃ H H —CH═CH—CH₂—CH₂— B-488 OCF₃ H H —CH═CH—CH₂—CH₂— B-489 H F H —CH═CH—CH₂—CH₂— B-490 F F H —CH═CH—CH₂—CH₂— B-491 Cl F H —CH═CH—CH₂—CH₂— B-492 Br F H —CH═CH—CH₂—CH₂— B-493 CH₃ F H —CH═CH—CH₂—CH₂— B-494 CF₃ F H —CH═CH—CH₂—CH₂— B-495 OCH₃ F H —CH═CH—CH₂—CH₂— B-496 OCF₃ F H —CH═CH—CH₂—CH₂— B-497 H Cl H —CH═CH—CH₂—CH₂— B-498 F Cl H —CH═CH—CH₂—CH₂— B-499 Cl Cl H —CH═CH—CH₂—CH₂— B-500 Br Cl H —CH═CH—CH₂—CH₂— B-501 CH₃ Cl H —CH═CH—CH₂—CH₂— B-502 CF₃ Cl H —CH═CH—CH₂—CH₂— B-503 OCH₃ Cl H —CH═CH—CH₂—CH₂— B-504 OCF₃ Cl H —CH═CH—CH₂—CH₂— B-505 H CH₃ H —CH═CH—CH₂—CH₂— B-506 F CH₃ H —CH═CH—CH₂—CH₂— B-507 Cl CH₃ H —CH═CH—CH₂—CH₂— B-508 Br CH₃ H —CH═CH—CH₂—CH₂— B-509 CH₃ CH₃ H —CH═CH—CH₂—CH₂— B-510 CF₃ CH₃ H —CH═CH—CH₂—CH₂— B-511 OCH₃ CH₃ H —CH═CH—CH₂—CH₂— B-512 OCF₃ CH₃ H —CH═CH—CH₂—CH₂— B-513 H CH₃ CH₃ —CH═CH—CH₂—CH₂— B-514 F CH₃ CH₃ —CH═CH—CH₂—CH₂— B-515 Cl CH₃ CH₃ —CH═CH—CH₂—CH₂— B-516 Br CH₃ CH₃ —CH═CH—CH₂—CH₂— B-517 CH₃ CH₃ CH₃ —CH═CH—CH₂—CH₂— B-518 CF₃ CH₃ CH₃ —CH═CH—CH₂—CH₂— B-519 OCH₃ CH₃ CH₃ —CH═CH—CH₂—CH₂— B-520 OCF₃ CH₃ CH₃ —CH═CH—CH₂—CH₂— B-521 H H —(CH₂)₃— CH₃ B-522 F H —(CH₂)₃— CH₃ B-523 Cl H —(CH₂)₃— CH₃ B-524 Br H —(CH₂)₃— CH₃ B-525 CH₃ H —(CH₂)₃— CH₃ B-526 CF₃ H —(CH₂)₃— CH₃ B-527 OCH₃ H —(CH₂)₃— CH₃ B-528 OCF₃ H —(CH₂)₃— CH₃ B-529 H D —(CH₂)₃— CH₃ B-530 F D —(CH₂)₃— CH₃ B-531 Cl D —(CH₂)₃— CH₃ B-532 Br D —(CH₂)₃— CH₃ B-533 CH₃ D —(CH₂)₃— CH₃ B-534 CF₃ D —(CH₂)₃— CH₃ B-535 OCH₃ D —(CH₂)₃— CH₃ B-536 OCF₃ D —(CH₂)₃— CH₃ B-537 H H —(CH₂)₃— D B-538 F H —(CH₂)₃— D B-539 Cl H —(CH₂)₃— D B-540 Br H —(CH₂)₃— D B-541 CH₃ H —(CH₂)₃— D B-542 CF₃ H —(CH₂)₃— D B-543 OCH₃ H —(CH₂)₃— D B-544 OCF₃ H —(CH₂)₃— D B-545 H D —(CH₂)₃— D B-546 F D —(CH₂)₃— D B-547 Cl D —(CH₂)₃— D B-548 Br D —(CH₂)₃— D B-549 CH₃ D —(CH₂)₃— D B-550 CF₃ D —(CH₂)₃— D B-551 OCH₃ D —(CH₂)₃— D B-552 OCF₃ D —(CH₂)₃— D B-553 H H —(CH₂)₄— CH₃ B-554 F H —(CH₂)₄— CH₃ B-555 Cl H —(CH₂)₄— CH₃ B-556 Br H —(CH₂)₄— CH₃ B-557 CH₃ H —(CH₂)₄— CH₃ B-558 CF₃ H —(CH₂)₄— CH₃ B-559 OCH₃ H —(CH₂)₄— CH₃ B-560 OCF₃ H —(CH₂)₄— CH₃ B-561 H D —(CH₂)₄— CH₃ B-562 F D —(CH₂)₄— CH₃ B-563 Cl D —(CH₂)₄— CH₃ B-564 Br D —(CH₂)₄— CH₃ B-565 CH₃ D —(CH₂)₄— CH₃ B-566 CF₃ D —(CH₂)₄— CH₃ B-567 OCH₃ D —(CH₂)₄— CH₃ B-568 OCF₃ D —(CH₂)₄— CH₃ B-569 H H —(CH₂)₄— D B-570 F H —(CH₂)₄— D B-571 Cl H —(CH₂)₄— D B-572 Br H —(CH₂)₄— D B-573 CH₃ H —(CH₂)₄— D B-574 CF₃ H —(CH₂)₄— D B-575 OCH₃ H —(CH₂)₄— D B-576 OCF₃ H —(CH₂)₄— D B-577 H D —(CH₂)₄— D B-578 F D —(CH₂)₄— D B-579 Cl D —(CH₂)₄— D B-580 Br D —(CH₂)₄— D B-581 CH₃ D —(CH₂)₄— D B-582 CF₃ D —(CH₂)₄— D B-583 OCH₃ D —(CH₂)₄— D B-584 OCF₃ D —(CH₂)₄— D *C₆H₅ = phenyl In a specific embodiment, the invention relates to compounds I selected from the compounds of the examples, either in form of free bases or of any pharmaceutically acceptable salt thereof or a steroisomer thereof.

The compounds of the present invention can be prepared by using routine techniques familiar to a skilled person. In particular, the compounds of the formula I can be prepared according to the following schemes, wherein the variables, if not stated otherwise, are as defined above.

Compounds of formula I wherein X is CR⁷R⁸ and R^(5b) is H (=compounds I′) can be synthesized as described in scheme 1 below. The protected tetrahydrobenzodiazepine or tetrahydroquinoxaline 1, wherein Z is a hydrogen or a halogen atom, such as Cl, Br or I and PG is a common protective group, such as a carbamate, especially boc, is acylated with the acrylic acid derivative 2, wherein LG is an appropriate leaving group, such as Cl or an anhydride or a chloroformate, in the presence of a base, such as triethylamine or Hünig's base, in an organic solvent, such as ether or methylene chloride. Reaction of 3 with a Lewis acid or a Brönstedt acid HA or irradiation with a suitable wavelength commonly derived from a mercury lamp in an adequate solvent, such as acetone or toluene, in a common photoreactor yields cyclization to 4. Reduction of the carbonyl group with common reduction agents like borohydrides such as sodium borohydride or borane-tetrahydrofurane-complex yields 5, which is deprotected using suitable reagents such as strong bases or acids to I′, wherein R^(4a) and R^(4b) and R^(5b) are H. Compounds I wherein R^(4a) and R^(4b) form together ═O can be obtained by skipping the reduction step to 5 and deprotecting 4.

If desired, substituents R¹ different from hydrogen can be introduced for example via alkylation under typical conditions such as stirring in an appropriate solvent in the presence of an alkylhalide and a base or via other common substitution reactions.

Compounds I wherein R^(5b) is different from H can be prepared, for example, by reacting compound 4 with a compound LG-R^(5b) in the presence of a base, wherein LG is an appropriate leaving group, such as Cl or Br.

Compounds I wherein R^(5b) is different from H and R⁸ is CH₃ (=compounds I″) can be prepared, for example, as out lined in scheme 2 below. Acylation of 1 with the allylic acid derivative 6, wherein LG is an appropriate leaving group, such as Cl or an anhydride or a chloroformate, in the presence of a base, such as triethylamine or Hünig's base, in an organic solvent, such as ether or methylene chloride, yields 7, which is reacted in a Heck-type reaction, e.g. employing palladium acetate in the presence of a base, such as potassium carbonate, to yield the cyclization product 8. Reduction of the carbonyl group with common reduction agents like borohydrides such as sodium borohydride or borane-tetrahydrofurane-complex yields 9, which is deprotected using suitable reagents such as strong bases or acids to I″, wherein R^(4a) and R^(4b) are H. Compounds I wherein R^(4a) and R^(4b) form together ═O can be obtained by skipping the reduction step to 9 and deprotecting 8. If desired, substituents R¹ different from hydrogen can be introduced for example via alkylation under typical conditions such as stirring in an appropriate solvent in the presence of an alkylhalide and a base or via other common substitution reactions.

Compounds I wherein X is NR⁶ (=compounds I′″) can be prepared as outlined in scheme 3 below. Acylation of 1 with the β-amino acid derivative 10, wherein PG′ is a protection group different from PG and LG is an appropriate leaving group, such as Cl or an anhydride or a chloroformate, in the presence of a base, such as triethylamine or Hünig's base, in an organic solvent, such as ether or methylene chloride, yields 11. This is first selectively deprotected at the amino group NR⁶PG′. The partially deprotected compound is then reacted in a cyclization reaction to 12 under Buchwald-Hartwig reaction conditions such as the use of a Pd catalyst, e.g. tetrakis(triphenylphosphine) palladium in the presence of as base, such as sodium tert-butylate and potassium carbonate. Reduction of the carbonyl group of 12 with common reduction agents like borohydrides such as sodium borohydride or borane-tetrahydrofurane-complex yields 13, which is deprotected using suitable reagents such as strong bases or acids to I′″, wherein R^(4a) and R^(4b) are H. Compounds I wherein R^(4a) and R^(4b) form together ═O can be obtained by skipping the reduction step to 13 and deprotecting 12. If desired, substituents R¹ different from hydrogen can be introduced for example via alkylation under typical conditions such as stirring in an appropriate solvent in the presence of an alkylhalide and a base or via other common substitution reactions.

Alternatively to the method depicted in scheme 1, compounds I wherein X is CR⁷R⁸ and R^(5b) is H (=compounds I′) can be synthesized as described in scheme 4 below. Readily available anilines 14 are derivatized with carbonyl moieties 15 by acylation procedures employing appropriate leaving groups LG, such as chlorides or anhydrides, in the presence of a base such as triethylamine or Hünig's base, in an organic solvent, such as diethyl ether or methylene chloride to yield 16. Cyclization products 17 are received by irradiation with a suitable wavelength commonly derived from a mercury lamp in an adequate solvent such as acetone or toluene in a common photoreactor known to those skilled in the art. Reduction with common reduction agents like borohydrides such as sodium borohydride or borane-tetrahydrofurane-complex yield suitable intermediates 18 that are alkylated with alkylamides 19 employing suitable leaving groups LG such as chlorides or bromides. After reduction to the corresponding amines 20 cyclization is performed in a suitable solvent like acetonitrile or methanol at room temperature or higher temperature by addition of an acid and substituted ketones or aldehydes to obtain compounds I′.

Alternatively to the method depicted in scheme 3, compounds I wherein X is NR⁶ (=compounds I′″) can be prepared as outlined in scheme 5 below.

Readily available starting materials 22 are alkylated with alkylamides 19 employing suitable leaving groups LG such as chlorides or bromides to give 23. After reduction to the corresponding amines 24 cyclization is performed in a suitable solvent like acetonitrile or methanol at room temperature or higher temperature by addition of an acid and substituted ketones or aldehydes 21 to obtain compounds I′″.

Compounds I wherein R^(4a) and R^(4b) are not H or do not form together a group ═O can be prepared by standard derivatization methods of compounds wherein R^(4a) and R^(4b) form together a group ═O. For instance, compounds wherein R^(4a) and R^(4b) form together a group ═S may be prepared by reaction with a sulfurization agent, such as Lawesson's reagent or P₂S₅. Alkyl and related groups as radicals R^(4a) and R^(4b) may be introduced via Grignard reduction. Amino and related groups may be introduced via reductive amination. Hydroxyl group R^(4a) or R^(4b) may be introduced by reducing the carbonyl group. This may be alkylated to yield alkoxy and related groups R^(4a) and R^(4b) or substituted by diverse groups.

If not otherwise indicated, the above-described reactions are generally carried out in a solvent at temperatures between room temperature and the boiling temperature of the solvent employed. Alternatively, the activation energy which is required for the reaction can be introduced into the reaction mixture using microwaves, something which has proved to be of value, in particular, in the case of the reactions catalyzed by transition metals (with regard to reactions using microwaves, see Tetrahedron 2001, 57, p. 9199 ff. p. 9225 ff. and also, in a general manner, “Microwaves in Organic Synthesis”, Andre Loupy (Ed.), Wiley-VCH 2002.

The acid addition salts of compounds I are prepared in a customary manner by mixing the free base with a corresponding acid, where appropriate in solution in an organic solvent, for example a lower alcohol, such as methanol, ethanol or propanol, an ether, such as methyl tert-butyl ether or diisopropyl ether, a ketone, such as acetone or methyl ethyl ketone, or an ester, such as ethyl acetate.

Routine experimentations, including appropriate manipulation of the reaction conditions, reagents and sequence of the synthetic route, protection of any chemical functionality that may not be compatible with the reaction conditions, and deprotection at a suitable point in the reaction sequence of the preparation methods are within routine techniques.

Suitable protecting groups and the methods for protecting and deprotecting different substituents using such suitable protecting groups are well known to those skilled in the art; examples of which may be found in T. Greene and P. Wuts, Protective Groups in Organic Synthesis (3^(rd) ed.), John Wiley & Sons, NY (1999), which is herein incorporated by reference in its entirety. Synthesis of the compounds of the invention may be accomplished by methods analogous to those described in the synthetic schemes described hereinabove and in specific examples.

Starting materials, if not commercially available, may be prepared by procedures selected from standard organic chemical techniques, techniques that are analogous to the synthesis of known, structurally similar compounds, or techniques that are analogous to the above described schemes or the procedures described in the synthetic examples section.

When an optically active form of a compound of the invention is required, it may be obtained by carrying out one of the procedures described herein using an optically active starting material (prepared, for example, by asymmetric induction of a suitable reaction step), or by resolution of a mixture of the stereoisomers of the compound or intermediates using a standard procedure (such as chromatographic separation, recrystallization or enzymatic resolution).

Similarly, when a pure geometric isomer of a compound of the invention is required, it may be obtained by carrying out one of the above procedures using a pure geometric isomer as a starting material, or by resolution of a mixture of the geometric isomers of the compound or intermediates using a standard procedure such as chromatographic separation.

Moreover, the present invention relates to compounds of formula I as defined above, wherein at least one of the atoms has been replaced by its stable, non-radioactive isotope (e.g., hydrogen by deuterium, ¹²C by ¹³C, ¹⁴N by ¹⁵N, ¹⁶O by ¹⁸O) and preferably wherein at least one hydrogen atom has been replaced by a deuterium atom.

Additionally, the compounds according to the invention include more of the respective isotope than occurs naturally occurs and which is present in compounds I.

Stable isotopes (e.g., deuterium, ¹³C, ¹⁵N, ¹⁸O) are nonradioactive isotopes which contain one additional neutron than the normally abundant isotope of the respective atom. Deuterated compounds have been used in pharmaceutical research to investigate the in vivo metabolic fate of the compounds by evaluation of the mechanism of action and metabolic pathway of the non deuterated parent compound (Blake et al. J. Pharm. Sci. 64, 3, 367-391 (1975)). Such metabolic studies are important in the design of safe, effective therapeutic drugs, either because the in vivo active compound administered to the patient or because the metabolites produced from the parent compound prove to be toxic or carcinogenic (Foster et al., Advances in Drug Research Vol. 14, pp. 2-36, Academic press, London, 1985; Kato et al., J. Labelled Comp. Radiopharmaceut., 36(10):927-932 (1995); Kushner et al., Can. J. Physiol. Pharmacol., 77, 79-88 (1999)).

Incorporation of a heavy atom, particularly substitution of deuterium for hydrogen, can give rise to an isotope effect that could alter the pharmacokinetics of the drug.

Stable isotope labeling of a drug can alter its physico-chemical properties such as pK_(a) and lipid solubility. These changes may influence the fate of the drug at different steps along its passage through the body. Absorption, distribution, metabolism or excretion can be changed. Absorption and distribution are processes that depend primarily on the molecular size and the lipophilicity of the substance. These effects and alterations can affect the pharmacodynamic response of the drug molecule if the isotopic substitution affects a region involved in a ligand-receptor interaction.

Drug metabolism can give rise to large isotopic effect if the breaking of a chemical bond to a deuterium atom is the rate limiting step in the process. While some of the physical properties of a stable isotope-labeled molecule are different from those of the unlabeled one, the chemical and biological properties are the same, with one important exception: because of the increased mass of the heavy isotope, any bond involving the heavy isotope and another atom will be stronger than the same bond between the light isotope and that atom. In any reaction in which the breaking of this bond is the rate limiting step, the reaction will proceed slower for the molecule with the heavy isotope due to “kinetic isotope effect”. A reaction involving breaking a C--D bond can be up to 700 percent slower than a similar reaction involving breaking a C—H bond. If the C--D bond is not involved in any of the steps leading to the metabolite, there may not be any effect to alter the behavior of the drug. If a deuterium is placed at a site involved in the metabolism of a drug, an isotope effect will be observed only if breaking of the C--D bond is the rate limiting step. There is evidence to suggest that whenever cleavage of an aliphatic C—H bond occurs, usually by oxidation catalyzed by a mixed-function oxidase, replacement of the hydrogen by deuterium will lead to observable isotope effect. It is also important to understand that the incorporation of deuterium at the site of metabolism slows its rate to the point where another metabolite produced by attack at a carbon atom not substituted by deuterium becomes the major pathway a process called “metabolic switching”.

Deuterium tracers, such as deuterium-labeled drugs and doses, in some cases repeatedly, of thousands of milligrams of deuterated water, are also used in healthy humans of all ages, including neonates and pregnant women, without reported incident (e.g. Pons G and Rey E, Pediatrics 1999 104: 633; Coward W A et al., Lancet 1979 7: 13; Schwarcz H P, Control. Clin. Trials 1984 5(4 Suppl): 573; Rodewald L E et al., J. Pediatr. 1989 114: 885; Butte N F et al. Br. J. Nutr. 1991 65: 3; MacLennan A H et al. Am. J. Obstet Gynecol. 1981 139: 948). Thus, it is clear that any deuterium released, for instance, during the metabolism of compounds of this invention poses no health risk.

The weight percentage of hydrogen in a mammal (approximately 9%) and natural abundance of deuterium (approximately 0.015%) indicates that a 70 kg human normally contains nearly a gram of deuterium. Furthermore, replacement of up to about 15% of normal hydrogen with deuterium has been effected and maintained for a period of days to weeks in mammals, including rodents and dogs, with minimal observed adverse effects (Czajka D M and Finkel A J, Ann. N.Y. Acad. Sci. 1960 84: 770; Thomson J F, Ann. New York Acad. Sci 1960 84: 736; Czakja D M et al., Am. J. Physiol. 1961 201: 357). Higher deuterium concentrations, usually in excess of 20%, can be toxic in animals. However, acute replacement of as high as 15%-23% of the hydrogen in humans' fluids with deuterium was found not to cause toxicity (Blagojevic N et al. in “Dosimetry & Treatment Planning for Neutron Capture Therapy”, Zamenhof R, Solares G and Harling O Eds. 1994. Advanced Medical Publishing, Madison Wis. pp. 125-134; Diabetes Metab. 23: 251 (1997)).

Increasing the amount of deuterium present in a compound above its natural abundance is called enrichment or deuterium-enrichment. Examples of the amount of enrichment include from about 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 12, 16, 21, 25, 29, 33, 37, 42, 46, 50, 54, 58, 63, 67, 71, 75, 79, 84, 88, 92, 96, to about 100 mol %.

The hydrogens present on a particular organic compound have different capacities for exchange with deuterium. Certain hydrogen atoms are easily exchangeable under physiological conditions and, if replaced by deuterium atoms, it is expected that they will readily exchange for protons after administration to a patient. Certain hydrogen atoms may be exchanged for deuterium atoms by the action of a deuteric acid such as D₂SO₄/D₂O. Alternatively, deuterium atoms may be incorporated in various combinations during the synthesis of compounds of the invention. Certain hydrogen atoms are not easily exchangeable for deuterium atoms. However, deuterium atoms at the remaining positions may be incorporated by the use of deuterated starting materials or intermediates during the construction of compounds of the invention.

Deuterated and deuterium-enriched compounds of the invention can be prepared by using known methods described in the literature. Such methods can be carried out utilizing corresponding deuterated and optionally, other isotope-containing reagents and/or intermediates to synthesize the compounds delineated herein, or invoking standard synthetic protocols known in the art for introducing isotopic atoms to a chemical structure. Relevant procedures and intermediates are disclosed, for instance in Lizondo, J et al., Drugs Fut, 21(11), 1116 (1996); Brickner, S J et al., J Med Chem, 39(3), 673 (1996); Mallesham, B et al., Org Lett, 5(7), 963 (2003); PCT publications WO1997010223, WO2005099353, WO1995007271, WO2006008754; U.S. Pat. Nos. 7,538,189; 7,534,814; 7,531,685; 7,528,131; 7,521,421; 7,514,068; 7,511,013; and US Patent Application Publication Nos. 20090137457; 20090131485; 20090131363; 20090118238; 20090111840; 20090105338; 20090105307; 20090105147; 20090093422; 20090088416; 20090082471, the methods are hereby incorporated by reference.

The present invention further relates to a pharmaceutical composition comprising a therapeutically effective amount of at least one compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof, or comprising at least one compound as defined in any of the preceding claims wherein at least one of the atoms has been replaced by its stable, non-radioactive isotope, preferably wherein at least one hydrogen atom has been replaced by a deuterium atom, in combination with at least one pharmaceutically acceptable carrier and/or auxiliary substance.

The present invention further relates to a compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for use as a medicament.

The present invention also relates to a compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for the treatment of disorders which respond to the modulation of the 5-HT_(2C) receptor.

The present invention also relates to the use of a compound I as defined above or of an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for the manufacture of a medicament for the treatment of disorders which respond to the modulation of the 5-HT_(2C) receptor, and to a method for treating disorders which respond to the modulation of the 5-HT_(2C) receptor, which method comprises administering to a subject in need thereof at least one compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof.

The compounds of the present invention are modulators of the 5-HT_(2C) receptor. Specifically, the compounds of formula I are agonists or partial agonists of the 5-HT₂c receptor. Thus, in a specific embodiment, the invention relates to a compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for the treatment of disorders which respond to 5-HT_(2c) receptor agonists, further to the use of a compound I as defined above or of an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for the manufacture of a medicament for the treatment of disorders which respond to 5-HT_(2c) receptor agonists, and to a method for treating disorders which respond to 5-HT_(2c) receptor agonists, which method comprises administering to a subject in need thereof at least one compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof.

Within the meaning of the invention, the term “disorder” denotes disturbances and/or anomalies which are as a rule regarded as being pathological conditions or functions and which can manifest themselves in the form of particular signs, symptoms and/or malfunctions. While the treatment according to the invention can be directed toward individual disorders, i.e. anomalies or pathological conditions, it is also possible for several anomalies, which may be causatively linked to each other, to be combined into patterns, i.e. syndromes, which can be treated in accordance with the invention.

In one aspect of the invention, the diseases to be treated are disorders are damage of the central nervous system, disorders of the central nervous system, eating disorders, ocular hypertension, cardiovascular disorders, gastrointestinal disorders and diabetes.

Disorders or diseases of the central nervous system are understood as meaning disorders which affect the spinal cord and, in particular, the brain. These are, for example, cognitive dysfunction, attention deficit disorder/hyperactivity syndrome and cognitive deficits related with schizophrenia, attention deficit/hyperactivity syndrome, personality disorders, affective disorders, motion or motor disorders, pain, migraine, sleep disorders (including disturbances of the Circadian rhythm), feeding disorders, diseases associated with neurodegeneration, addiction diseases, obesity or psoriasis.

Examples of cognitive dysfunction are deficits in memory, cognition, and learning, Alzheimer's disease, age-related cognitive decline, and mild cognitive impairment, or any combinations thereof. Examples of personality disorders are schizophrenia and cognitive deficits related to schizophrenia. Examples of affective disorders are depression, anxiety, bipolar disorder and obsessive compulsive disorders, or any combination thereof. Examples of motion or motor disorders are Parkinson's disease and epilepsy. Examples of feeding disorders are obesity, bulimia, weight loss and anorexia, especially anorexia nervosa. Examples of diseases associated with neurodegeneration are stroke, spinal or head trauma, and head injuries, such as hydrocephalus.

Pain condition includes nociceptive pain, neuropathic pain or a combination thereof. Such pain conditions or disorders can include, but are not limited to, post-operative pain, osteoarthritis pain, pain due to inflammation, rheumatoid arthritis pain, musculoskeletal pain, burn pain (including sunburn), ocular pain, the pain associated with dental conditions (such as dental caries and gingivitis), post-partum pain, bone fracture, herpes, HIV, traumatic nerve injury, stroke, post-ischemia, fibromyalgia, reflex sympathetic dystrophy, complex regional pain syndrome, spinal cord injury, sciatica, phantom limb pain, diabetic neuropathy, hyperalgesia and cancer.

In certain other embodiments, the disease condition is bladder dysfunction, including urinary incontinence.

Diabetes includes diabetes insipidus, diabetes mellitus, type I diabetes, type II diabetes, type III diabetes, diabetes secondary to pancreatic diseases, diabetes related to steroid use, diabetes complications, hyperglycemia and insulin resistance.

The addiction diseases include psychiatric disorders and behavioral disturbances which are caused by the abuse of psychotropic substances, such as pharmaceuticals or narcotics, and also other addiction diseases, such as addiction to gaming (impulse control disorders not elsewhere classified). Examples of addictive substances are: opioids (e.g. morphine, heroin and codeine), cocaine; nicotine; alcohol; substances which interact with the GABA chloride channel complex, sedatives, hypnotics and tranquilizers, for example benzodiazepines; LSD; cannabinoids; psychomotor stimulants, such as 3,4-methylenedioxy-N-methylamphetamine (ecstasy); amphetamine and amphetamine-like substances such as methylphenidate, other stimulants including caffeine and nicotine. Addictive substances which come particularly into consideration are opioids, cocaine, amphetamine or amphetamine-like substances, nicotine and alcohol. Especially, addiction disorders include alcohol abuse, cocaine abuse, tobacco abuse and smoking cessation.

With regard to the treatment of addiction diseases, particular preference is given to those compounds according to the invention of the formula (I) which themselves do not possess any psychotropic effect. This can also be observed in a test using rats, which, after having been administered compounds which can be used in accordance with the invention, reduce their self administration of psychotropic substances, for example cocaine.

Examples of gastrointestinal disorders are irritable bowel syndrome.

Preferably, the disorders are selected from the group consisting of bipolar disorder, depression, atypical depression, mood episodes, adjustment disorders, anxiety, panic disorders, post-traumatic syndrome, psychoses, schizophrenia, cognitive deficits of schizophrenia, memory loss, dementia of aging, Alzheimer's disease, behavioral disorders associated with dementia, social phobia, mental disorders in childhood, attention deficit hyperactivity disorder, organic mental disorders, autism, mutism, disruptive behavior disorder, impulse control disorder, borderline personality disorder, obsessive compulsive disorder, migraine and other conditions associated with cephalic pain or other pain, raised intracranial pressure, seizure disorders, epilepsy, substance use disorders, alcohol abuse, cocaine abuse, tobacco abuse, smoking cessation, sexual dysfunction/erectile dysfunction in males, sexual dysfunction in females, premenstrual syndrome, late luteal phase syndrome, chronic fatigue syndrome, sleep disorders, sleep apnoea, chronic fatigue syndrome, psoriasis, Parkinson's disease, spinal cord injury, trauma, stroke, pain, bladder dysfunction/urinary incontinence, encephalitis, meningitis, eating disorders, obesity, bulimia, weight loss, anorexia nervosa, ocular hypertension, cardiovascular disorders, gastrointestinal disorders, diabetes insipidus, diabetes mellitus, type I diabetes, type II diabetes, type III diabetes, diabetes secondary to pancreatic diseases, diabetes related to steroid use, diabetes complications, hyperglycemia and insulin resistance, and are specifically schizophrenia, depression, bipolar disorders, obesity or substance use disorders.

The compounds of the invention may be used for a preventive treatment (prophylaxis), in particular as relapse prophylaxis or phase prophylaxis, but are preferably used for a treatment in its proper sense, i.e. for the treatment of acute or chronic signs, symptoms and/or malfunctions. The treatment can be orientated symptomatically, for example as the suppression of symptoms. It can be effected over a short period, be orientated over the medium term or can be a long-term treatment, for example within the context of a maintenance therapy.

In another embodiment, the present invention relates to the use of a compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for preparing a medicament for preventing (the development of) a disease condition as described above and to a method for preventing (the development of) a disease condition as described above comprises administering to the subject in need of treatment thereof (e.g., a mammal, such as a human) a therapeutically effective amount of a compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof. As used herein, the term “prevent” a disease condition by administration of any of the compounds described herein means that the detectable physical characteristics or symptoms of the disease or condition do not develop following the administration of the compound described herein. Alternatively, the method comprises administering to the subject a therapeutically effective amount of a compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof, in combination with a therapeutically effective amount of at least one cognitive enhancing drug.

In yet another embodiment, the present invention relates to the use a compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof for preparing a medicament for preventing the progression (e.g., worsening) of a disease condition and to a method for preventing the progression (e.g., worsening) of a disease condition, which method comprises administering to the subject in need of treatment thereof (e.g., a mammal, such as a human) a therapeutically effective amount of a compound I as defined above or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof.

There are several lines of evidence suggesting that 5-HT_(2C) agonists or partial agonists would have therapeutic use in a variety of diseases, disorders and conditions.

Knockout mice models lacking the 5-HT_(2C) receptor exhibit hyperphagia, obesity and are more prone to seizures and sudden death [Tecott L H, Sun L M, Akana S F, Strack A M, Lowenstein D H, Dallman M F, Julius D (1995) Eating disorder and epilepsy in mice lacking 5-HT_(2C) serotonin receptors. Nature 374:542-546]. They also exhibit compulsive-like behavior [Chou-Green J M, Holscher T D, Dallman M F, Akana S F (2003). Compulsive behavior in the 5-HT_(2C) receptor knockout mouse. Phys. Behav. 78:641-649], hyperresponsiveness to repeated stress [Chou-Green J M, Holscher T D, Dallman M F, Akana S F (2003). Repeated stress in young and old 5-HT_(2C) receptor knockout mouse. Phys. Behav. 79:217-226], wakefulness [Frank M G, Stryker M P, Tecott L H (2002). Sleep and sleep homeostasis in mice lacking the 5-HT_(2C) receptor. Neuropsychopharmacology 27:869-873], hyperactivity and drug dependence [Rocha B A, Goulding E H, O'Dell L E, Mead A N, Coufal N G, Parsons L H, Tecott L H (2002). Enhanced locomotor, reinforcing and neurochemical effects of cocaine in serotonin 5-hydroxytryptamine 2C receptor mutant mice. J. Neurosci. 22:10039-10045].

5-HT_(2C) is unique among other G-protein-coupled receptors (GPCRs) in that its pre-mRNA is a substrate for base modification via hydrolytic deamination of adenosines to yield inosines. Five adenosines, located within a sequence encoding the putative second intracellular domain can be converted to inosines. This editing can alter the coding potential of the triplet codons and allows for the generation of multiple different receptor isoforms. The edited receptor isoforms were shown to have reduced ability to interact with G-proteins in the absence of agonist stimulation [Werry, T D, Loiacono R, Sexton P A, Christopoulos A (2008). RNA editing of the serotonin 5-HT_(2C) receptor and its effects on cell signaling, pharmacology and brain function. Pharmac. Therap. 119:7-23].

Edited 5-HT_(2C) isoforms with reduced function are significantly expressed in the brains of depressed suicide victims [Schmauss C (2003) Serotonin 2C receptors: suicide, serotonin, and runaway RNA editing. Neuroscientist 9:237-242. Iwamoto K, Kato T (2003). RNA editing of serotonin 2C receptor in human postmortem brains of major mental disorders. Neurosci. Lett. 346:169-172] and in the learned helplessness rats (a well established animal model of depression) [Iwamotoa K, Nakatanib N, Bundoa M, Yoshikawab T, Katoa T (2005). Altered RNA editing of serotonin 2C receptor in a rat model of depression. Neurosci. Res. 53: 69-76] suggesting a link between 5-HT_(2C) function and depression. There are also implications of edited 5-HT_(2C) isoforms and spatial memory [Du Y, Stasko M, Costa A C, Davissone M T, Gardiner K J (2007). Editing of the serotonin 2C receptor pre-mRNA Effects of the Morris Water Maze. Gene 391:186-197]. In addition, fully edited isoforms of the human 5-HT_(2C) receptor display a striking reduction in sensitivity to lysergic acid diethylamide (LSD) and to atypical antipsychotic drugs clozapine and loxapine, suggesting a possible role of the receptor in the etiology and pharmacology of schizophrenia [Niswender C M, Herrick-Davis K., Dilley G E, Meltzer H Y, Overholser J C, Stockmeier C A, Emeson R B, Sanders-Bush E (2001). RNA Editing of the Human Serotonin 5-HT_(2C) Receptor: Alterations in Suicide and Implications for Serotonergic Pharmacotherapy. Neuropsychopharm. 24:478-491].

Recently, the availability of potent and selective 5-HT_(2C) receptor agonists made it possible to directly investigate the effects of 5-HT_(2C) agonists and their therapeutic potential. Thus recent studies demonstrated that selective 5-HT_(2C) agonists resulted in decreased food intake and body weight gain in normal and obese rats [Smith B M, et al. (2008). Discovery and structure-activity relationship of (1R)-8-chloro-2,3,4,5-tetrahydro-1-methyl-1H-3-benzazepine (Lorcaserin), a selective serotonin 5-HT_(2C) receptor agonist for the treatment of obesity. J Med Chem 51:305-313. Thomsen W J, Grottick A J, Menzaghi F, Reyes-Saldana H, Espitia S, Yuskin D, Whelan K, Martin M, Morgan M, Chen W, Al-Shama H, Smith B, Chalmers D, Behan D (2008) Lorcaserin, A Novel Selective Human 5-HT_(2C) Agonist: In Vitro and In Vivo Pharmacological Characterization. J Pharmacol Exp Ther. 325:577-587. Rosenzweig-Lipson S, Zhang J, Mazandarani H, Harrison B L, Sabb A, Sabalski J, Stack G, Welmaker G, Barrett J E, Dunlop J (2006) Antiobesity-like effects of the 5-HT_(2C) receptor agonist WAY-161503. Brain Res. 1073-1074:240-251. Dunlop J, Sabb A L, Mazandarani H, Zhang J, Kalgaonker S, Shukhina E, Sukoff S, Vogel R L, Stack G, Schechter L, Harrison B L, Rosenzweig-Lipson S (2005). WAY-163909 [97bR, 10aR)-1,2,3,4,8,9,10,10a-octahydro-7bH-cyclopenta-[b][1,4]diazepino[6,7,1hi]indole], a novel 5-hydroxytryptamine 2C receptor—selective agonist with anorectic activity. J Pharmacol Exp Ther. 313:862-869.].

Furthermore, selective 5-HT_(2C) receptor agonists produce antidepressant effects in animal models of depression comparable to those of SSRIs but with a much faster onset of action and a therapeutic window that avoids antidepressant-induced sexual dysfunction. These agonists were also effective in animal models of compulsive behavior such as scheduled induced polydipsia and they also exhibited decreased hyperactivity and aggression in rodents [Rosenzweig-Lipson S, Sabb A, Stack G, Mitchell P, Lucki I, Malberg J E, Grauer S, Brennan J, Cryan J F, Sukoff Rizzo S J, Dunlop J, Barrett J E, Marquis K L (2007) Antidepressant-like effects of the novel, selective, 5-HT_(2C) receptor agonist WAY-163909 in rodents. Psychopharmacology (Berlin) 192:159-170. Rosenzweig-Lipson S, Dunlop J, Marquis K L (2007) 5-HT_(2C) receptor agonists as an innovative approach for psychiatric disorders. Drug news Perspect, 20: 565-571. Cryan, J F, Lucki I (2000). Antidepressant-like behavioral effects mediated by 5-Hydroxytryptamine 2C receptors. J. Pharm. Exp. Ther. 295:1120-1126.].

Acute or chronic administration of 5-HT_(2C) agonists decreases the firing rate of ventral tegmental area dopamine neurons but not that of substantia nigra. In addition 5-HT_(2C) agonists reduce dopamine levels in the nucleus accumbens but not in the striatum (the region of the brain mostly associated with extrapyramidal side effects) [Di Matteo, V., Di Giovanni, G., Di Mascio, M., & Esposito, E. (1999). SB 242084, a selective serotonin 2C receptor antagonist, increases dopaminergic transmission in the mesolimbic system. Neuropharmacology 38, 1195-1205. Di Giovanni, G., Di Matteo, V., Di Mascio, M., & Esposito, E. (2000). Preferential modulation of mesolimbic vs. nigrostriatal dopaminergic function by serotonin 2C/2B receptor agonists: a combined in vivo electrophysiological and microdialysis study. Synapse 35, 53-61. Marquis K L, Sabb A L, Logue S F, Brennan J A, Piesla M J, Comery T A, Grauer S M, Ashby C R, Jr., Nguyen H Q, Dawson L A, Barrett J E, Stack G, Meltzer H Y, Harrison B L, Rosenzweig-Lipson S (2007) WAY-163909 [(7bR,10aR)-1,2,3,4,8,9,10,10a-octahydro-7bH-cyclopenta-[b][1,4]diazepino[6,7,1hi]indole]: A novel 5-hydroxytryptamine 2C receptor-selective agonist with preclinical antipsychotic-like activity. J Pharmacol Exp Ther 320:486-496.]. Therefore it is expected that 5-HT_(2C) receptor agonists will selectively decrease mesolimibic dopamine levels without affecting the nigrostriatal pathway thus avoiding the EPS side effects of typical antipsychotics. Several 5-HT_(2C) receptor agonists have shown antipsychotic activity in animal models of schizophrenia without EPS based on the lack of effect in catalepsy [Marquis K L, Sabb A L, Logue S F, Brennan J A, Piesla M J, Comery T A, Grauer S M, Ashby C R, Jr., Nguyen H Q, Dawson L A, Barrett J E, Stack G, Meltzer H Y, Harrison B L, Rosenzweig-Lipson S (2007) WAY-163909 [(7bR,10aR)-1,2,3,4,8,9,10,10a-octahydro-7bH-cyclopenta-[b][1,4]diazepino[6,7,1hi]indole]: A novel 5-hydroxytryptamine 2C receptor-selective agonist with preclinical antipsychotic-like activity. J Pharmacol Exp Ther 320:486-496. Siuciak J A, Chapin D S, McCarthy S A, Guanowsky V, Brown J, Chiang P, Marala R, Patterson T, Seymour P A, Swick A, Iredale P A (2007) CP-809,101, a selective 5-HT_(2C) agonist, shows activity in animal models of antipsychotic activity. Neuropharmacology 52:279-290]. The antipsychotic activity of 5-HT_(2C) receptor agonists without EPS coupled with their beneficial effects in mood disorders and cognition and their antiobesity like effects render 5-HT_(2C) receptor agonists as unique agents to treat schizophrenia [Rosenzweig-Lipson S, Dunlop J, Marquis K L (2007) 5-HT_(2C) receptor agonists as an innovative approach for psychiatric disorders. Drug news Perspect, 20: 565-571. Dunlop J, Marquis K L, Lim H K, Leung L, Kao J, Cheesman C, Rosenzweig-Lipson S (2006). Pharmacological profile of the 5-HT_(2C) receptor agonist WAY-163909; therapeutic potential in multiple indications. CNS Dug Rev. 12:167-177.].

In addition 5-HT_(2C) modulation has been implicated in epilepsy [Isaac M (2005). Serotonergic 5-HT_(2C) receptors as a potential therapeutic target for the antiepileptic drugs. Curr. Topics fed. Chem. 5:59:67], psoriasis [Thorslund K, Nordlind K (2007). Serotonergic drugs-a possible role in the treatment of psoriasis? Drug News Perspect 20:521-525], Parkinson's disease and related motor disorders [Esposito E, Di Matteo V, Pierucci M, Benigno A, Di Giavanni, G (2007). Role of central 5-HT_(2C) receptor in the control of basal ganglia functions. The Basal Ganglia Pathophysiology: Recent Advances 97-127], behavioral deficits [Barr A M, Lahmann-Masten V, Paulus M, Gainetdinov R P, Caron M G, Geyer M A (2004). The selective serotonin-2A receptor antagonist M100907 reverses behavioral deficits in dopamine transporter knockout mice. Neuropsychopharmacology 29:221-228], anxiety [Dekeyne A, Mannoury la Cour C, Gobert A, Brocco M, Lejuene F, Serres F, Sharp T, Daszuta A, Soumier A, Papp M, Rivet J M, Flik G, Crerners T I, Muller O, Lavielle G, Millan M J (2208). S32006, a novel 5-HT_(2C) receptor antagonists displaying broad-based antidepressant and anxiolytic properties in rodent models. Psychopharmacology 199:549-568. Nunes-de-Souza V, Nunes-de-Souza R L, Rodgers R J, Canto-de-Souza A (2008). 5-HT2 receptor activation in the midbrain periaqueductal grey (PAG) reduces anxiety-like behavior in mice. Behav. Brain Res. 187:72-79.], migraine [Leone M, Rigamonti A, D'Amico D, Grazzi L, Usai S, Bussone G (2001). The serotonergic system in migraine. Journal of Headache and Pain 2(Suppl. 1):S43-S46], Alzheimer's disease [Arjona A A, Pooler A M, Lee R K, Wurtman R J (2002). Effect of a 5-HT_(2C) serotonin agonist, dexnorfenfluramine, on amyloid precursor protein metabolism in guinea pigs. Brain Res. 951:135-140], pain and spinal cord injury [Nakae A, Nakai K, Tanaka T, Hagihira S, Shibata M, Ueda K, Masimo T (2008). The role of RNA editing of the serotonin 2C receptor in a rat model of oro-facial neuropathic pain. The European Journal of Neuroscience 27:2373-2379. Nakae A, Nakai K, Tanaka T, Takashina M, Hagihira S, Shibata M, Ueda K, Mashimo T (2008). Serotonin 2C receptor mRNA editing in neuropathic pain model. Neurosci. Res. 60:228-231. Kao T, Shumsky J S, Jacob-Vadakot S, Timothy H B, Murray M, Moxon, K A (2006). Role of the 5-HT_(2C) receptor in improving weight-supported stepping in adult rats spinalized as neonates. Brain Res. 1112:159-168.], sexual dysfunction [Motofei I G (2008). A dual physiological character for sexual function: the role of serotonergic receptors. BJU International 101:531-534. Shimada I, Maeno K, Kondoh Y, Kaku H, Sugasawa K, Kimura Y, Hatanaka K; Naitou Y, Wanibuchi F, Sakamoto S; Tsukamoto S (2008). Synthesis and structure-activity relationships of a series of benzazepine derivatives as 5-HT₂c receptor agonists. Bioorg. Med. Chem. 16:3309-3320.], smoking cessation [Fletcher P J, Le A D, Higgins G A (2008). Serotonin receptors as potential targets for modulation of nicotine use and dependence. Progress Brain Res. 172:361-83], substance dependence [Bubar M J, Cunningham K A (2008). Prospects for serotonin 5-HT2R pharmacotherapy in psychostimulant abuse. Progress Brain Res. 172:319-46], and ocular hypertension [Sharif N A, McLaughlin M A, Kelly C R (2006). AL-34662: a potent, selective, and efficacious ocular hypotensive serotonin-2 receptor agonist. J Ocul Pharmacol Ther. 23:1-13].

Further, 5HT modulation can be useful in the treatment of pain, both neuropathic and nociceptive pain, see for example U.S. Patent application publication US2007/0225277. Obata, Hideaki; Ito, Naomi; Sasaki, Masayuki; Saito, Shigeru; Goto, Fumio. Possible involvement of spinal noradrenergic mechanisms in the antiallodynic effect of intrathecally administered 5-HT2C receptor agonists in the rats with peripheral nerve injury. European Journal of Pharmacology (2007), 567(1-2), 89-94. Serotonin2C receptor mRNA editing in neuropathic pain model. Nakae, Aya; Nakai, Kunihiro; Tanaka, Tatsuya; Takashina, Masaki; Hagihira, Satoshi; Shibata, Masahiko; Ueda, Koichi; Mashimo, Takashi. Department of Anesthesiology & Intensive Care Medicine, Graduate School of Medicine, Osaka University, Neuroscience Research (Amsterdam, Netherlands) (2008), 60(2), 228-231. Antiallodynic effects of intrathecally administered 5-HT2C receptor agonists in rats with nerve injury. Obata, Hideaki; Saito, Shigeru; Sakurazawa, Shinobu; Sasaki, Masayuki; Usui, Tadashi; Goto, Fumio. Department of Anesthesiology, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan. Pain (2004), 108(1-2), 163-169. Influence of 5,7-dihydroxytryptamine (5,7-DHT) on the antinociceptive effect of serotonin (5-HT) 5-HT2C receptor agonist in male and female rats. Brus, Ryszard; Kasperska, Alicja; Oswiecimska, Joanna; Szkilnik, Ryszard. Department of Pharmacology, Silesian Medical University, Zabrze, Pol. Medical Science Monitor (1997), 3(5), 654-656.

Modulation of 5HT2 receptors may be beneficial in the treatment of conditions related to bladder function, in particular, urinary incontinence. [Discovery of a novel azepine series of potent and selective 5-HT2C agonists as potential treatments for urinary incontinence. Brennan, Paul E.; Whitlock, Gavin A.; Ho, Danny K. H.; Conlon, Kelly; McMurray, Gordon. Bioorganic & Medicinal Chemistry Letters (2009), 19(17), 4999-5003. Investigation of the role of 5-HT2 receptor subtypes in the control of the bladder and the urethra in the anesthetized female rat. Mbaki, Y.; Ramage, A. G. Department of Pharmacology, University College London, London, UK. British Journal of Pharmacology (2008), 155(3), 343-356.] In particular, compounds with agonist activity at 5-HT_(2C) have been shown to be useful in treating urinary incontinence, see for example U.S. Patent application publications US2008/0146583 and US 2007/0225274.

In the use and the method of the invention, an effective quantity of one or more compounds, as a rule formulated in accordance with pharmaceutical and veterinary practice, is administered to the individual to be treated, preferably a mammal, in particular a human being, productive animal or domestic animal. Whether such a treatment is indicated, and in which form it is to take place, depends on the individual case and is subject to medical assessment (diagnosis) which takes into consideration signs, symptoms and/or malfunctions which are present, the risks of developing particular signs, symptoms and/or malfunctions, and other factors.

Actual dosage levels of active ingredients in the pharmaceutical compositions of the present invention can be varied so as to obtain an amount of the active compound(s) that is effective to achieve the desired therapeutic response for a particular subject (e.g., a mammal, preferably, a human (patient)), compositions and mode of administration. The selected dosage level will depend upon the activity of the particular compound, the route of administration, the severity of the condition being treated and the condition and prior medical history of the patient being treated. However, it is within the skill of the art to start doses of the compound at levels lower than required to achieve the desired therapeutic effect and to gradually increase the dosage until the desired effect is achieved.

Compounds of the present invention can also be administered to a subject as a pharmaceutical composition comprising the compounds of interest in combination with at least one pharmaceutically acceptable carriers. The phrase “therapeutically effective amount” of the compound of the present invention means a sufficient amount of the compound to treat disorders, at a reasonable benefit/risk ratio applicable to any medical treatment. It will be understood, however, that the total daily usage of the compounds and compositions of the present invention will be decided by the attending physician within the scope of sound medical judgment. The specific therapeutically effective dose level for any particular patient will depend upon a variety of factors including the disorder being treated and the severity of the disorder; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, sex and diet of the patient; the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidental with the specific compound employed; and like factors well-known in the medical arts. For example, it is well within the skill of the art to start doses of the compound at levels lower than required to achieve the desired therapeutic effect and to gradually increase the dosage until the desired effect is achieved.

The total daily dose of the compounds of this invention administered to a subject (namely, a mammal, such as a human) ranges from about 0.01 mg/kg body weight to about 100 mg/kg body weight. More preferable doses can be in the range of from about 0.01 mg/kg body weight to about 30 mg/kg body weight. If desired, the effective daily dose can be divided into multiple doses for purposes of administration. Consequently, single dose compositions may contain such amounts or submultiples thereof to make up the daily dose.

In one aspect, the present invention provides pharmaceutical compositions. The pharmaceutical compositions of the present invention comprise the compounds of the present invention or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt or solvate thereof. The pharmaceutical compositions of the present invention comprise compounds of the present invention that can be formulated together with at least one non-toxic pharmaceutically acceptable carrier.

In yet another embodiment, the present invention provides a pharmaceutical composition comprising compounds of the present invention or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable carriers, alone or in combination with one or more compounds that are not the compounds of the present invention. Examples of one or more compounds that can be combined with the compounds of the present invention in pharmaceutical compositions, include, but are not limited to, one or more cognitive enhancing drugs.

The pharmaceutical compositions of this present invention can be administered to a subject (e.g., a mammal, such as a human) orally, rectally, parenterally, intracisternally, intravaginally, intraperitoneally, topically (as by powders, ointments or drops), bucally or as an oral or nasal spray. The term “parenterally” as used herein, refers to modes of administration which include intravenous, intramuscular, intraperitoneal, intrasternal, subcutaneous and intraarticular injection and infusion.

The term “pharmaceutically acceptable carrier” as used herein, means a non-toxic, inert solid, semi-solid or liquid filler, diluent, encapsulating material or formulation auxiliary of any type. Some examples of materials which can serve as pharmaceutically acceptable carriers are sugars such as, but not limited to, lactose, glucose and sucrose; starches such as, but not limited to, corn starch and potato starch; cellulose and its derivatives such as, but not limited to, sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients such as, but not limited to, cocoa butter and suppository waxes; oils such as, but not limited to, peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols; such a propylene glycol; esters such as, but not limited to, ethyl oleate and ethyl laurate; agar; buffering agents such as, but not limited to, magnesium hydroxide and aluminum hydroxide; alginic acid; pyrogen-free water; isotonic saline; Ringer's solution; ethyl alcohol, and phosphate buffer solutions, as well as other non-toxic compatible lubricants such as, but not limited to, sodium lauryl sulfate and magnesium stearate, as well as coloring agents, releasing agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the composition, according to the judgment of the formulator.

Pharmaceutical compositions of the present invention for parenteral injection comprise pharmaceutically acceptable sterile aqueous or nonaqueous solutions, dispersions, suspensions or emulsions as well as sterile powders for reconstitution into sterile injectable solutions or dispersions just prior to use. Examples of suitable aqueous and nonaqueous carriers, diluents, solvents or vehicles include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol and the like), vegetable oils (such as olive oil), injectable organic esters (such as ethyl oleate) and suitable mixtures thereof. Proper fluidity can be maintained, for example, by the use of coating materials such as lecithin, by the maintenance of the required particle size in the case of dispersions and by the use of surfactants.

These compositions may also contain adjuvants such as preservatives, wetting agents, emulsifying agents and dispersing agents. Prevention of the action of microorganisms can be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid and the like. It may also be desirable to include isotonic agents such as sugars, sodium chloride and the like.

Prolonged absorption of the injectable pharmaceutical form can be brought about by the inclusion of agents which delay absorption such as aluminum monostearate and gelatin.

In some cases, in order to prolong the effect of the drug, it is desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This can be accomplished by the use of a liquid suspension of crystalline or amorphous material with poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle.

Injectable depot forms are made by forming microencapsule matrices of the drug in biodegradable polymers such as polylactide-polyglycolide. Depending upon the ratio of drug to polymer and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions which are compatible with body tissues.

The injectable formulations can be sterilized, for example, by filtration through a bacterial-retaining filter or by incorporating sterilizing agents in the form of sterile solid compositions which can be dissolved or dispersed in sterile water or other sterile injectable medium just prior to use.

Solid dosage forms for oral administration include capsules, tablets, pills, powders and granules. In such solid dosage forms, the active compound may be mixed with at least one inert, pharmaceutically acceptable excipient or carrier, such as sodium citrate or dicalcium phosphate and/or a) fillers or extenders such as starches, lactose, sucrose, glucose, mannitol and silicic acid; b) binders such as carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidone, sucrose and acacia; c) humectants such as glycerol; d) disintegrating agents such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates and sodium carbonate; e) solution retarding agents such as paraffin; f) absorption accelerators such as quaternary ammonium compounds; g) wetting agents such as cetyl alcohol and glycerol monostearate; h) absorbents such as kaolin and bentonite clay and i) lubricants such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate and mixtures thereof. In the case of capsules, tablets and pills, the dosage form may also comprise buffering agents.

Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such carriers as lactose or milk sugar as well as high molecular weight polyethylene glycols and the like.

The solid dosage forms of tablets, dragees, capsules, pills and granules can be prepared with coatings and shells such as enteric coatings and other coatings well-known in the pharmaceutical formulating art. They may optionally contain opacifying agents and may also be of a composition such that they release the active ingredient(s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of embedding compositions which can be used include polymeric substances and waxes.

The active compounds can also be in micro-encapsulated form, if appropriate, with one or more of the above-mentioned carriers.

Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups and elixirs. In addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art such as, for example, water or other solvents, solubilizing agents and emulsifiers such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethyl formamide, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor and sesame oils), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan and mixtures thereof.

Besides inert diluents, the oral compositions may also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring and perfuming agents.

Suspensions, in addition to the active compounds, may contain suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar, tragacanth and mixtures thereof.

Compositions for rectal or vaginal administration are preferably suppositories which can be prepared by mixing the compounds of this invention with suitable non-irritating carriers or carriers such as cocoa butter, polyethylene glycol or a suppository wax which are solid at room temperature but liquid at body temperature and therefore melt in the rectum or vaginal cavity and release the active compound.

Compounds of the present invention can also be administered in the form of liposomes. As is known in the art, liposomes are generally derived from phospholipids or other lipid substances. Liposomes are formed by mono- or multi-lamellar hydrated liquid crystals which are dispersed in an aqueous medium. Any non-toxic, physiologically acceptable and metabolizable lipid capable of forming liposomes can be used. The present compositions in liposome form can contain, in addition to a compound of the present invention, stabilizers, preservatives, excipients and the like. The preferred lipids are natural and synthetic phospholipids and phosphatidyl cholines (lecithins) used separately or together.

Methods to form liposomes are known in the art. See, for example, Prescott, Ed., Methods in Cell Biology, Volume XIV, Academic Press, New York, N.Y. (1976), p. 33 et seq.

Dosage forms for topical administration of a compound of the present invention include powders, sprays, ointments and inhalants. The active compound may be mixed under sterile conditions with a pharmaceutically acceptable carrier and any needed preservatives, buffers or propellants which may be required. Ophthalmic formulations, eye ointments, powders and solutions are also contemplated as being within the scope of this invention.

The compounds of the present invention can be used in the form of pharmaceutically acceptable salts derived from inorganic or organic acids. The phrase “pharmaceutically acceptable salt” means those salts which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response and the like and are commensurate with a reasonable benefit/risk ratio.

Pharmaceutically acceptable salts are well known in the art. For example, S. M. Berge et al. describe pharmaceutically acceptable salts in detail in (J. Pharmaceutical Sciences, 1977, 66: 1 et seq.). The salts can be prepared in situ during the final isolation and purification of the compounds of the invention or separately by reacting a free base function with a suitable organic acid. Representative acid addition salts include, but are not limited to acetate, adipate, alginate, citrate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, camphorate, camphorsulfonate, digluconate, glycerophosphate, hemisulfate, heptanoate, hexanoate, fumarate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethansulfonate (isothionate), lactate, malate, maleate, methanesulfonate, nicotinate, 2-naphthalenesulfonate, oxalate, palmitoate, pectinate, persulfate, 3-phenylpropionate, picrate, pivalate, propionate, succinate, tartrate, thiocyanate, phosphate, glutamate, bicarbonate, p-toluenesulfonate and undecanoate. Also, the basic nitrogen-containing groups can be quaternized with such agents as lower alkyl halides such as, but not limited to, methyl, ethyl, propyl, and butyl chlorides, bromides and iodides; dialkyl sulfates like dimethyl, diethyl, dibutyl and diamyl sulfates; long chain halides such as, but not limited to, decyl, lauryl, myristyl and stearyl chlorides, bromides and iodides; arylalkyl halides like benzyl and phenethyl bromides and others. Water or oil-soluble or dispersible products are thereby obtained. Examples of acids which can be employed to form pharmaceutically acceptable acid addition salts include such inorganic acids as hydrochloric acid, hydrobromic acid, sulfuric acid, and phosphoric acid and such organic acids as acetic acid, fumaric acid, maleic acid, 4-methylbenzenesulfonic acid, succinic acid and citric acid.

Basic addition salts can be prepared in situ during the final isolation and purification of compounds of this invention by reacting a carboxylic acid-containing moiety with a suitable base such as, but not limited to, the hydroxide, carbonate or bicarbonate of a pharmaceutically acceptable metal cation or with ammonia or an organic primary, secondary or tertiary amine. Pharmaceutically acceptable salts include, but are not limited to, cations based on alkali metals or alkaline earth metals such as, but not limited to, lithium, sodium, potassium, calcium, magnesium and aluminum salts and the like and nontoxic quaternary ammonia and amine cations including ammonium, tetramethylammonium, tetraethylammonium, methylammonium, dimethylammonium, trimethylammonium, triethylammonium, diethylammonium, ethylammonium and the like. Other representative organic amines useful for the formation of base addition salts include ethylenediamine, ethanolamine, diethanolamine, piperidine, piperazine and the like.

The compounds of the present invention can exist in unsolvated as well as solvated forms, including hydrated forms, such as hemi-hydrates. In general, the solvated forms, with pharmaceutically acceptable solvents such as water and ethanol among others are equivalent to the unsolvated forms for the purposes of the invention.

The following examples serve to explain the invention without limiting it.

EXAMPLES

The compounds were either characterized via proton-NMR in d₆-dimethylsulfoxide or d-chloroform or d₄-methanol on a 400 MHz or 500 MHz NMR instrument (Bruker AVANCE), or by mass spectrometry, generally recorded via HPLC-MS in a fast gradient on C18-material (electrospray-ionisation (ESI) mode).

The magnetic nuclear resonance spectral properties (NMR) refer to the chemical shifts (6) expressed in parts per million (ppm). The relative area of the shifts in the ¹H-NMR spectrum corresponds to the number of hydrogen atoms for a particular functional type in the molecule. The nature of the shift, as regards multiplicity, is indicated as singlet (s), broad singlet (s. br.), doublet (d), broad doublet (d br.), triplet (t), broad triplet (t br.), quartet (q), quintet (quint.) and multiplet (m).

Enantiomers were separated/purified either by chiral supercritical fluid chromatography (SFC) (method A) or by chiral HPLC (method B).

Method A—Chiral Analytical SFC

Analytical SFC was performed on an Aurora A5 SFC Fusion and Agilent 1100 system running under Agilent Chemstation software control. The SFC system included a 10-way column switcher, CO2 pump, modifier pump, oven, and backpressure regulator. The mobile phase comprised of supercritical CO2 supplied by a beverage-grade CO2 cylinder with a modifier mixture of methanol at a flow rate of 3 mL/min. Oven temperature was at 35° C. and the outlet pressure at 150 bar. The UV detector was set to collect at wavelengths of 220 nm and 254 nm. The mobile phase gradient started with 5% modifier and held it for 0.1 minutes at a flow rate of 1 mL/min, then the flow rate was ramped up to 3 mL/min and held for 0.4 min. The modifier was ramped from 5% to 15% over the next 8 minutes at 3 mL/min then held for 1 minute at 15% modifier (3 mL/min). The gradient was ramped down from 15% to 5% modifier over 0.5 min (3 mL/min). The instrument was fitted with a Chiralpak AS-H column with dimensions of 4.6 mm i.d.×150 mm length with 5 μm particles.

Method B—Chiral HPLC

System: KNAUER preparative HPLC Pump: Preparative pump 1800 Detector: Smartline UV detector 2600 257 nm Sample pump: Knauer HPLC-Pump K-120 Fractional collector: Smartline Valves Drive S6

Software: ChromGate® V3.1.7, KNAUER Instrument Control Column: Whelk O 4.6 mm ID×250 mm

Column temperature: 25° C. Mobile phase: hexane/isopropylamine 95/5 Flow rate: 1 ml/min

I. PREPARATION EXAMPLES Example 1 8,8-Dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-1 of Table B) 1.1 Preparation of tert-butyl 1-(3-methylbut-2-enoyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate

1 g (4.04 mmol) of tert-butyl 2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate was dissolved in 20 mL of dichloromethane and treated with 1.54 mL (8.86 mL) of triethylamine followed by 0.53 mL (4.83 mmol) of 3-methylbut-2-enoyl chloride. The reaction mixture was stirred over night at room temperature, poured onto water (50 mL) and extracted three times with 50 mL of dichloromethane each. The organic phases were combined, washed with a saturated solution of sodium chloride, dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 5-10% methanol in dichloromethane) to yield 1.27 g of the title compound as a white solid.

ESI-MS: m/z (%): 275.10 (100, [M-C₄H₉+H]⁺).

1.2 Preparation of tert-butyl 8,8-dimethyl-6-oxo-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline-2(6H)-carboxylate

A solution of 0.33 g (1.0 mmol) of tert-butyl 1-(3-methylbut-2-enoyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate of step 1.1 was irradiated with a 150 W mercury lamp in an immersion well reactor with a pyrex filter in 20 mL of acetone until completion of the reaction monitored by liquid chromatography. The solution was concentrated in vacuo and the residue was purified by column chromatography on silica (eluent: 10-30% ethyl acetate in heptane) to yield 202 mg of the title compound as a beige solid.

ESI-MS: m/z (%): 275.10 (100, [M-C₄H₉+H]⁺).

1.3 Preparation of tert-butyl 8,8-dimethyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline-2(6H)-carboxylate

A solution of 38 mg (0.115 mmol) tert-butyl 8,8-dimethyl-6-oxo-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline-2(6H)-carboxylate of step 1.2 in 1 mL of tetrahydrofuran was treated with 0.46 mL of 1 molar solution of borohydride-tetrahydrofuran complex in tetrahydrofuran. The mixture was stirred over night, and then quenched with water and diluted hydrochloric acid. The pH was adjusted to pH 9 by addition of aqueous sodium hydroxide solution and the mixture extracted three times with 10 mL of dichloromethane each. The solution was dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 20-30% ethyl acetate in heptane) to yield 21 mg of the title compound as a clear oil.

ESI-MS: m/z (%): 317.20 (100, [M+H]⁺).

1.4 Preparation of 8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline

287 mg (0.9 mmol) of tert-butyl 8,8-dimethyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline-2(6H)-carboxylate of step 1.3 were dissolved in 5 mL of dichloromethane and treated with 2.5 mL of trifluoroacetic acid. The mixture was stirred over night at room temperature and then extracted once with water (10 mL). The organic phase was then extracted twice with a diluted solution of sodium hydroxide (10 mL each), dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 10-30% methanol in dichloromethane) to yield 141 mg of the title compound as a yellow oil.

ESI-MS: m/z (%): 217.15 (100, [M+H]⁺).

¹H-NMR (500 MHz, CDCl₃): δ=7.15 (d, 1H), 6.85 (d, 1H), 6.75 (m, 1H), 3.80 (s, 2H), 3.15 (m, 2H), 3.00 (s, 4H), 1.65 (m, 2H), 1.20 (s, 6H).

Example 2 1,2,3,4-Tetrahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopent[2]en]-6(7H)-one 2,2,2-trifluoroacetate (Compound of the Formula I.j, I.k or I.1 in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-481 of Table B) 2.1 Preparation of tert-butyl 6-oxo-3,4,6,7-tetrahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopent[2]ene]-2(1H)-carboxylate (Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-401 of Table B, Wherein However R¹ is not H, but Boc)

A solution of 50 mg (0.128 mmol) tert-butyl 9-chloro-1-(2-cyclopentenylacetyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate was dissolved in 1 mL of degassed dry acetonitrile under argon, treated with 1.4 mg (0.006 mmol) of palladium acetate, 6.10 mg (0.013 mmol) dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine and 53 mg (0.384 mmol) potassium carbonate. The mixture was stirred for 10 hours at 120° C. in a synthesis microwave system. After cooling to room temperature the mixture was filtered over celite, diluted with dichloromethane and then extracted twice with a diluted solution of sodium chloride (10 mL each), dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 10-30% ethyl acetate in heptane) to yield 40 mg of the title compound as a yellow oil.

ESI-MS: m/z (%): 299.10 (100, [M-C₄H₉+H]⁺).

2.2 Preparation of 1,2,3,4-tetrahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopent[2]en]-6(7H)-one 2,2,2-trifluoroacetate

Boc-deprotection of the compound obtained in step 2.1 analogously to example 1.4 yielded the title compound.

ESI-MS: m/z (%): 255 (100, [M+H]⁺).

Example 3 8-Methyl-8-phenyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one, hydrochloride (Compound of the Formula I.j, I.k or I.l in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-161 of Table B)

392 mg (1 mmol) of tert-butyl 1-(3-phenylbut-2-enoyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate were treated with 1 g of polyphosphoric acid. The mixture was heated to 90° C. for 2 hours and then quenched with a saturated solution of potassium carbonate at 0° C. The mixture was extracted three times with ethyl acetate (20 mL each), the combined organic fractions dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 10-30% methanol in dichloromethane) to yield 86 mg of the title compound as a yellow foam.

ESI-MS: m/z (%): 293.1 (100, [M+H]⁺).

1H-NMR (500 MHz, DMSO-d6): δ=10.05 (bs, 1H), 9.85 (bs, 1H), 7.40 (d, 1H), 7.35 (d, 1H), 7.25 (m, 2H), 7.20 (m, 2H), 7.10 (m, 2H), 4.55 (m, 1H), 4.35 (m, 1H), 4.15 (m, 1H), 3.55 (m, 1H), 3.25 (m, 2H), 3.10 (m, 1H), 2.70 (m, 1H), 1.60 (s, 3H).

The following example was prepared analogously to example 1.

Example 4 8,8-Dimethyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one (Compound of the Formula I.j, I.k or I.l in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-1 of Table B)

ESI-MS: m/z (%): 231 (100, [M+H]⁺).

1H-NMR (500 MHz, CDCl₃): δ=7.20 (d, 1H), 7.00 (m, 2H), 4.10 (s, 4H), 3.20 (m, 2H), 2.50 (s, 2H), 1.30 (s, 6H).

The following examples 5 and 6 were prepared analogously to example 2.

Example 5 1,2,3,4-Tetrahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopentan]-6(7H)-one (Compound of the Formula I.j, I.k or I.l in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-361 of Table B)

ESI-MS: m/z (%): 257 (100, [M+H]⁺).

Example 6 1,2,3,4,6,7-Hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopentane](Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-361 of Table B)

ESI-MS: m/z (%): 243 (100, [M+H]⁺).

¹H-NMR (500 MHz, CDCl₃): δ=7.15 (d, 1H), 6.95 (d, 1H), 6.80 (m, 1H), 3.90 (s, 2H), 3.20 (m, 2H), 3.05 (m, 4H), 1.95-1.65 (m, 10H).

The following examples 7 to 13 were prepared analogously to example 1.

Example 7 12a-Methyl-4,5,6,7,10,11,12,12a-octahydrocyclopenta[c][1,4]diazepino[6,7,1-ij]quinolin-9(9aH)-one (Racemic Cis Diastereomer of the Compound of the Formula I.j, I.k or I.l in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-521 of Table B)

ESI-MS: m/z (%): 257 (100, [M+H]⁺).

Example 8 8-Methyl-8-(trifluoromethyl)-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (Single Enantiomer of the Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-81 of Table B)

ESI-MS: m/z (%): 271 (100, [M+H]⁺).

The retention time according to method A is 1.396 min.

Example 9 8-Methyl-8-(trifluoromethyl)-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (Single Enantiomer of the Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-81 of Table B)

ESI-MS: m/z (%): 271 (100, [M+H]⁺).

The retention time according to method A is 1.543 min.

Example 10 12a-Methyl-4,5,6,7,10,11,12,12a-octahydrocyclopenta[c][1,4]diazepino[6,7,1-ij]quinolin-9(9aH)-one (Racemic Trans Diastereomer of the Compound of the Formula I.j, I.k or I.l in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-521 of Table B)

ESI-MS: m/z (%): 257 (100, [M+H]⁺).

Example 11 12a-Methyl-4,5,6,7,9,9a, 10,11,12,12a-decahydrocyclopenta[c][1,4]diazepino[6,7,1-ij]quinoline (Racemic Cis Diastereomer of the Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-521 of Table B)

ESI-MS: m/z (%): 243 (100, [M+H]⁺).

¹H-NMR (500 MHz, CDCl₃): δ=7.15 (d, 1H), 6.90 (d, 1H), 6.80 (m, 1H), 3.90 (m, 2H), 3.15 (m, 1H), 3.05 (m, 3H), 2.95 (m, 1H), 2.80 (m, 1H), 1.95 (m, 1H), 1.90 (m, 1H), 1.80 (m, 2H), 1.60 (m, 1H), 1.55 (m, 1H), 1.30 (m, 1H), 1.20 (s, 3H).

Example 12 8-Methyl-8-(trifluoromethyl)-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one (Racemic Mixture of Compound of the Formula I.j, I.k or 1.1 in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-81 of Table B)

ESI-MS: m/z (%): 285 (100, [M+H]⁺).

Example 13 12a-Methyl-4,5,6,7,9,9a,10,11,12,12a-decahydrocyclopenta[c][1,4]diazepino-[6,7,1-ij]quinoline hydrochloride (Racemic Trans Diastereomer of the Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-521 of Table B)

ESI-MS: m/z (%): 243 (100, [M+H]⁺).

¹H-NMR (500 MHz, CDCl₃): δ=9.45 (bs, 1H), 9.05 (bs, 1H), 7.05 (d, 1H), 7.00 (d, 1H), 6.70 (m, 1H), 4.30 (m, 1H), 3.95 (m, 1H), 3.55 (m, 2H), 3.35 (m, 1H), 3.25 (m, 2H), 2.95 (m, 1H), 1.95 (m, 1H), 1.85 (m, 1H), 1.80 (m, 1H), 1.70 (m, 1H), 1.55 (m, 1H), 1.40 (m, 1H), 1.25 (m, 1H), 0.90 (s, 3H).

The following examples 14 and 15 were prepared analogously to example 3.

Example 14 8-Methyl-8-phenyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline hydrochloride (Racemic Mixture in Form of the Salt of the Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-161 of Table B)

ESI-MS: m/z (%): 279 (100, [M+H]⁺)

¹H-NMR (500 MHz, CDCl₃): δ=7.22-7.27 (m, 2H), 7.11-7.19 (m, 3H), 6.95-7.04 (m, 2H), 6.78 (dd, J=8.0, 7.5 Hz, 1H), 3.99 (d, J=14.4 Hz, 1H), 3.87 99 (d, J=14.5 Hz, 1H), 3.20-3.26 (m, 1H), 3.01-3.08 (m, 4H), 2.87-2.94 (m, 1H), 2.09-2.15 (m, 1H), 1.92-1.99 (m, 1H), 1.73 (s, 3H) ppm.

Example 15 8-Methyl-8-phenyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (Racemic Mixture of Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R and R^(9a) is as in Row B-161 of Table B)

ESI-MS: m/z (%): 279 (100, [M+H]⁺).

¹H NMR (CDCl₃, 500 MHz): [ppm]: 7.25 (m, 2H), 7.15 (m, 3H), 7.05 (d, 1H), 6.95 (d, 1H), 6.80 (m, 1H), 4.00 (m, 1H), 3.90 (m, 1H), 3.25 (m, 1H), 3.05 (m, 4H), 2.90 (m, 1H), 2.10 (m, 1H), 1.95 (m, 1H), 1.75 (s, 3H).

Example 16 (R)-5,6,7,9,9a, 10,11,12-Octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (2,2,2-trifluoroacetate) (R-Enantiomer of the Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row A-865 of Table A) 16.1 Preparation of (R)-tert-butyl 9-oxo-6,7,9a, 10,11,12-hexahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline-5(9H)-carboxylate

65 mg of (R)-tert-butyl 9-chloro-1-(pyrrolidine-2-carbonyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate was stirred together with 1.8 mg of 2′-(di-tert-butylphosphino)-N,N-dimethylbiphenyl-2-amine, 2.5 mg Pd₂(dba)₃ and 19 mg sodium 2-methylpropan-2-olate at 100° C. over 10 hours in toluene. The reaction mixture was then cooled to room temperature and evaporated. The residue was purified by column chromatography on silica (eluent: 10-25% ethyl acetate in heptane) to yield 20 mg of the title compound as a beige solid.

ESI-MS: m/z (%): 344.20 (100, [M+H]⁺).

16.2 Preparation of (R)-tert-butyl 6,7,9a, 10,11,12-hexahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline-5(9H)-carboxylate (R-Enantiomer of the Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row A-121 of Table a, Wherein However R¹ is not H, but Boc)

Reduction of the compound obtained in step 16.1 analogously to example 1.3 yielded the title compound.

ESI-MS: m/z (%): 330.20 (100, [M+H]⁺).

16.3 Preparation of (R)-5,6,7,9,9a,10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline bis(2,2,2-trifluoroacetate) (R-Enantiomer of the Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row A-121 of Table A)

Boc-deprotection of the compound obtained in step 16.2 analogously to example 1.4 yielded the title compound.

ESI-MS: m/z (%): 230.15 (100, [M+H]⁺).

Example 17 was prepared analogously to example 16 employing (S)-tert-butyl 9-chloro-1-(pyrrolidine-2-carbonyl)-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate as starting material which was derived from (R)-1-(((9H-fluoren-9-yl)methoxy)carbonyl)pyrrolidine-2-carboxylic acid.

Example 17 (S)-5,6,7,9,9a, 10,11,12-Octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (2,2,2-trifluoroacetate) (S-Enantiomer of the Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row A-865 of Table A)

ESI-MS: m/z (%): 230 (100, [M+H]⁺).

The following examples 18 to 23 were prepared analogously to example 1.

Example 18 9-Chloro-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline, (2,2,2-trifluoroacetate) (Compound of the Formula I.g in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-3 of Table B)

ESI-MS: m/z (%): 251 (100, [M+H]⁺).

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 8.95 (bs, 2H), 7.35 (d, 1H), 7.25 (d, 1H), 4.15 (s, 2H), 3.30-3.20 (m, 6H), 1.65 (m, 2H), 1.25 (s, 6H).

Example 19 10-Chloro-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (2,2,2-trifluoroacetate) (Compound of the Formula I.h in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-3 of Table B)

ESI-MS: m/z (%): 251 (100, [M+H]⁺).

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 9.10 (bs, 2H), 7.35 (m, 1H), 7.20 (m, 1H), 4.15 (s, 2H), 3.30-3.20 (m, 6H), 1.65 (m, 2H), 1.25 (s, 6H).

Example 20 9-Chloro-8,8-dimethyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one 2,2,2-trifluoroacetate (Compound of the Formula I.j in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-3 of Table B)

ESI-MS: m/z (%): 265 (100, [M+H]⁺).

Example 21 10-Chloro-8,8-dimethyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one 2,2,2-trifluoroacetate (Compound of the Formula I.k in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-3 of Table B)

ESI-MS: m/z (%): 265 (100, [M+H]⁺).

Example 22 9-Fluoro-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (Compound of the Formula I.g in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-2 of Table B)

ESI-MS: m/z (%): 235 (100, [M+H]⁺).

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.95 (m, 1H), 6.55 (m, 1H), 3.95 (s, 2H), 3.20-3.10 (m, 6H), 1.70 (m, 2H), 1.40 (s, 6H).

Example 23 10-Fluoro-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (2,2,2-trifluoroacetate) (Compound of the Formula I.h in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-2 of Table B)

ESI-MS: m/z (%): 235 (100, [M+H]⁺).

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 9.05 (bs, 2H), 7.05 (d, 1H), 6.80 (m, 1H), 4.20 (s, 2H), 3.35 (m, 2H), 3.30 (m, 3.25), 3.25 (m, 2H), 1.70 (m, 2H), 1.30 (s, 6H).

The following examples 24 to 26 were prepared analogously to example 2.

Example 24 1,2,3,4,6,7-Hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclohexane] (2,2,2-trifluoroacetate) (Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-401 of Table B)

ESI-MS: m/z (%): 257.2 (100, [M+H]⁺).

¹H NMR (CDCl₃, 500 MHz): [ppm]: 8.85 (bs, 2H), 7.45 (d, 1H), 7.15 (d, 1H), 6.90 (m, 1H), 4.15 (s, 2H), 3.25 (m, 4H), 3.15 (m, 2H), 1.80 (m, 2H), 1.70 (m, 4H), 1.55 (m, 4H), 1.30 (m, 2H).

Example 25 1′,2′,3′,4′,6′,7′-Hexahydrospiro[cyclobutane-1,8′-[1,4]diazepino[6,7,1-ij]quinoline], hydrochloride (Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-321 of Table B)

ESI-MS [M+H⁺]=229.20

¹H NMR (CDCl₃, 500 MHz): [ppm]: 8.80 (bs, 2H), 7.50 (d, 1H), 6.95 (d, 1H), 6.90 (m, 1H), 4.10 (s, 2H), 3.25 (m, 2H), 3.20 (m, 2H), 3.10 (m, 2H), 2.35 (m, 2H), 2.00 (m, 2H), 1.90 (m, 4H).

Example 26 9′-Fluoro-1′,2′,3′,4′,6′,7′-hexahydrospiro[cyclobutane-1,8′-[1,4]diazepino[6,7,1-ij]quinoline], hydrochloride (Compound of the Formula I.g in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-322 of Table B)

ESI-MS [M+H⁺]=247.15

¹H NMR (DMSO-d₆, 500 MHz): [ppm]: 9.00 (bs, 2H), 7.25 (m, 1H), 6.80 (m, 1H), 4.10 (s, 2H), 3.25 (m, 2H), 3.20 (m, 2H), 3.10 (m, 2H), 2.65 (m, 2H), 2.00 (m, 4H), 1.85 (m, 2H).

The following examples 27 and 28 were prepared analogously to example 1.

Example 27 Enantiomer of 7,8,8-trimethyl-1,2,3,4,7,8-hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline](Enantiomer of the Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in row B-25 of Table B)

ESI-MS [M+H⁺]=231.20

¹H NMR (CDCl₃, 500 MHz): [ppm]: 7.25 (d, 1H), 7.00 (d, 1H), 6.85 (dd, 1H), 4.00 (m, 1H), 3.90 (m, 1H), 3.15 (m, 4H), 3.05 (m, 2H), 1.85 (m, 1H), 1.30 (s, 3H), 1.10 (s, 3H), 0.95 (d, 3H).

The retention time of the Boc-protected precursor according to method B is 10.363.

Example 28 Enantiomer of 7,8,8-trimethyl-1,2,3,4,7,8-hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline](Enantiomer of the Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-25 of Table B)

ESI-MS [M+H⁺]=231.20

¹H NMR (CDCl₃, 500 MHz): [ppm]: 7.25 (d, 1H), 7.00 (d, 1H), 6.85 (dd, 1H), 4.00 (m, 1H), 3.90 (m, 1H), 3.15 (m, 4H), 3.05 (m, 2H), 1.85 (m, 1H), 1.30 (s, 3H), 1.10 (s, 3H), 0.95 (d, 3H).

The retention time of the Boc-protected precursor according to method B is 11.410 min.

The following example 29 was prepared analogously to example 1.

Example 29 3-Methyl-1′,2′,3′,4′,6′,7′-hexahydrospiro[cyclobutane-1,8′-[1,4]diazepino[6,7,1-ij]quinoline], hydrochloride (Compound of the Formula I.p, I.q or I.r in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-321 of Table B)

ESI-MS [M+H⁺]=243.20

¹H NMR (DMSO-d₆, 500 MHz): [ppm]: 9.30 (bs, 1H), 8.55 (bs, 1H), 7.60 (d, 1H), 7.20 (d, 1H), 6.95 (dd, 1H), 4.20 (m, 1H), 4.05 (m, 1H), 3.35 (m, 1H), 3.20 (m, 2H), 2.90 (m, 1H), 2.40 (m, 1H), 2.25 (m, 1H), 2.05 (m, 1H), 1.95 (m, 6H), 1.2 (d, 3H).

Example 30 3-Benzyl-2′,3′,7′,8′,9′,10′-hexahydro-1H-3′,8′,10a′-triaza-cyclohepta[de]naphthalene (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row A-181 of Table A) 30.1 Preparation of 2-(4-benzyl-3,4-dihydro-2H-quinoxalin-1-yl)-acetamide

A solution of 1 g (4.46 mmol) 1-benzyl-1,2,3,4-tetrahydroquinoxaline in 10 ml of dimethylformamide was treated with 3.14 ml (18.15 mmol) of N-Ethyl-N-isopropylpropan-2-amine, and subsequently 863 mg (9.23 mmol) 2-chloroacetamide was added. The reaction mixture was heated in a microwave system at 100° C. for four hours. The resulting mixture was quenched with water and extracted once with ethylacetate. The aqueous phase was set to pH 10 with sodium hydroxide solution and extracted 3× with ethylacetate. The combined organic extracts were dried with magnesium sulfate, evaporated till dryness and directly purified by column chromatography on silica (eluent: starting with heptane and then up to 100% ethylacetate) to yield 1.224 g of the title compound.

ESI-MS: m/z (%): 282.10 (100, [M+H]⁺).

30.2 Preparation of 2-(4-Benzyl-3,4-dihydro-2H-quinoxalin-1-yl)-ethylamine

To 1.224 g (4.35 mmol) of 2-(4-benzyl-3,4-dihydro-2H-quinoxalin-1-yl)-acetamide were added 10.88 ml (21.75 mmol) borane dimethylsulfide THF solution and subsequently heated to 60° C. for six hours in a microwave system. The mixture was quenched with 1 molar hydrochloric acid and methanol and heated for 15 minutes at 60° C. in a microwave system. The reaction mixture was diluted with ethylacetate and extracted 3× with 1 molar hydrochlorid acid. The combined aqueous phases were set to pH 10 with sodium hydroxide solution and extracted 3× with dichloromethane. The combined organic phases were dried and evaporated to yield 1.089 g of the title compound as an oil.

ESI-MS: m/z (%): 268.15 (100, [M+H]⁺).

30.3 Preparation of 3-benzyl-2,3,7,8,9,10-hexahydro-1H-3,8,10a-triaza-cyclohepta[de]-naphthalene

A solution of 1.089 g (4.07 mmol) of 2-(4-benzyl-3,4-dihydro-2H-quinoxalin-1-yl)-ethylamine and 20 ml ethanol was treated with 122 mg (4.07 mmol) of formaldehyde and 511 mg (4.48 mmol) of trifluoroacetic acid and stirred over night at room temperature. The solvent was evaporated and dichloromethane was added to the crude mixture. The organic phase was washed with 1 molar sodium hydroxide solution. The organic phase was dried and purified by column chromatography on silica (eluent: starting with dichloromethane and then up to 100% methanol) to yield 448 mg of the title compound.

ESI-MS [M+H⁺]=280.10 (100, [M+H]⁺).

¹H NMR (CDCl₃, 500 MHz): [ppm]: 7.35 (m, 3H), 7.30 (m, 2H), 6.80 (dd, 1H), 6.65 (d, 1H), 6.60 (d, 1H), 4.55 (s, 2H), 4.10 (s, 2H), 3.30 (m, 4H), 3.25 (m, 2H), 3.10 (m, 2H).

Example 31 9-Fluoro-1-methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane], Trifluoroacetic Acid Salt (Compound of the Formula I.m in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-322 of Table B) 31.1 Preparation of 2-cyclobutylidene-N-(3-fluorophenyl)-acetamide

1.5 g (13.50 mmol) of 3-fluoroaniline were dissolved in 20 ml of dichloromethane and treated with 5.19 g (29.7 mmol) of N-ethyl-N-isopropylpropan-2-amine. Within 10 min 12.82 g (16.20 mmol) of 2-cyclobutylideneacetyl chloride were added at 0° C. and the solution was stirred overnight at room temperature. The mixture was poured on ice water and extracted 2× with dichloromethane. The combined organic phases were washed once with saturated sodium chloride solution, dried with MgSO₄ and evaporated in vacuo. The crude oil was treated with heptane and decanted twice, redissolved in ether-dichloromethane and treated with heptane till crystallization, yielding 2.2 g (77%) of a beige solid.

ESI-MS: m/z (%): 206 (100, [M+H]⁺).

31.2 Preparation of 5′-fluoro-1′H-spiro[cyclobutane-1,4′-quinolin]-2′(3′H)-one

A solution of 400 mg (1.94 mmol) of 2-cyclobutylidene-N-(3-fluorophenyl)-acetamide obtained in step 31.1 was dissolved in 19.5 ml of toluene and irradiated with a Hg middle pressure lamp in a suitable device till completion of the reaction indicated by liquid chromatography. The crude solution was concentrated in vacuo and the residue was purified by column chromatography on silica (eluent: 10-30% ethyl acetate in heptane) to yield 55 mg (14%) of the title compound as a beige solid.

ESI-MS: m/z (%): 206 (100, [M+H]⁺).

31.3 Preparation of 5′-fluoro-2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinoline]

A solution of 50 mg (0.244 mmol) of 5′-fluoro-1′H-spiro[cyclobutane-1,4′-quinolin]-2′(3′H)-one obtained in step 31.2 in 1 mL of tetrahydrofuran was treated with 0.73 mL of 1 M solution of borohydride-tetrahydrofuran complex in tetrahydrofuran. The mixture was stirred at reflux for 2 h, quenched with water and evaporated till dryness. The crude compound was used in the subsequent step without purification.

ESI-MS: m/z (%): 192 (100, [M+H]⁺).

31.4 Preparation of 2-(5′-fluoro-2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinolin]-1′-yl)-acetamide

A solution of 50 mg (0.26 mmol) of 5′-fluoro-2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinoline] obtained in step 31.3 in 1 ml of dimethylformamide was treated with 6.2 mg (0.26 mmol) of sodium hydride followed by 72 mg (0.52 mmol) 2-bromoacetamide and heated in a microwave system at 100° C. for one hour. The resulting mixture was quenched with water, evaporated till dryness and directly purified by column chromatography on silica (eluent: 10% methanol in dichloromethane) to yield 70 mg of the title compound with about 80% purity determined by LCMS.

ESI-MS: m/z (%): 249 (100, [M+H]⁺).

31.5 Preparation of 2-(5′-fluoro-2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinolin]-1′-yl)ethanamine

A solution of 40 mg (0.16 mmol) of 2-(5′-fluoro-2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinolin]-1′-yl)-acetamide obtained in step 31.4 in 1 ml of tetrahydrofurane was treated with 38 μl (0.38 mmol) of borane dimethylsulfide and heated to 70° C. for two hours. The mixture was quenched with water and hydrochloric acid, diluted with dichloromethane and extracted twice with water. The combined aqueous phases were set to pH 10 with sodium hydroxide solution and extracted 3× with dichloromethane. The combined organic phases were dried and evaporated to yield 10 mg of the title compound as an oil.

ESI-MS: m/z (%): 235 (100, [M+H]⁺).

31.6 Preparation of 9-fluoro-1-methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane], Trifluoroacetic Acid Salt

A solution of 10 mg (0.043 mmol) of 2-(5′-fluoro-2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinolin]-1′-yl)ethan-amine obtained in step 31.5 in 0.4 ml of acetonitrile/methanol was treated with 3.8 mg (0.085 mmol) of acetaldehyde and 6.5 μl (0.085 mmol) of trifluoroacetic acid and stirred over night at room temperature. The solvent was evaporated and the crude mixture purified with reversed phase liquid chromatography to yield 1.5 mg of the title compound as beige solid.

ESI-MS: m/z (%): 261 (100, [M+H]⁺).

¹H-NMR (500 MHz, pyridine-d5): δ=7.05 (dd, 1H), 6.80 (dd, 1H), 4.20 (q, 1H), 3.05 (m, 2H), 3.00 (m, 2H), 2.85 (m, 2H), 2.75 (m, 2H), 2.05 (m, 2H), 1.90-1.70 (m, 4H), 1.50 (d, 3H) ppm.

Example 32 2,3,5,6,7,8-Hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-217 of Table A) 32.1 Preparation of tert-butyl 1-benzyl-2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate

To a solution of 388 mg (1.39 mmol) of 1-benzyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (compound of example 30) in 15 ml of dichloromethane was treated with 0.49 ml (2.78 mmol) of N,N-diisopropylethylamine. 333 mg (1.53 mmol) of di-tert-butyl dicarbonate were dissolved in 5 ml of dichloromethane, slowly added to the reaction mixture and the solution was then stirred overnight at room temperature. The solution was diluted with dichloromethane and treated twice with 10% aqueous solution of citric acid. The organic phase was washed once with saturated sodium chloride solution, dried with MgSO₄ and concentrated in vacuo, yielding 559 mg of the crude product. The crude compound was used in the subsequent step without purification.

ESI-MS [M+H⁺]=380.20

32.2 Preparation of tert-butyl 2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]-quinoxaline-7(8H)-carboxylate

559 mg (1.47 mmol) of tert-butyl 1-benzyl-2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate (559 mg, 1,473 mmol) (from step 32.1) were dissolved in 10 ml of methanol. The solution was hydrogenated with a 10% Pd/C cartridge using the H-Cube apparatus (from Thales Nano) at 80 bar and 70° C. with a flow rate of 0.5 ml/min for 6 hours. The solution was concentrated in vacuo yielding 320 mg of the crude product. The crude compound was used in the subsequent step without purification.

ESI-MS [M+H⁺]=290.20

32.3 Preparation of 2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline

30 mg (0.104 mmol) of tert-butyl 2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate (from step 32.2) were dissolved in 2 ml of dichloromethane and treated with 0.20 ml (2.59 mmol) of trifluoroacetic acid at 0° C. The solution was allowed to warm up to room temperature and stirred for 2 h. The reaction mixture was diluted with dichloromethane and extracted once with a 1 molar aqueous solution of sodium hydroxide. The aqueous phase was extracted 3× with ethyl acetate. The combined organic phases were dried with magnesium sulfate, and concentrated in vacuo yielding 14 mg (0.076 mmol) of the title compound.

ESI-MS [M+H⁺]=190.10

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.75 (m, 1H), 6.55 (d, 1H), 6.50 (d, 1H), 3.90 (s, 2H), 3.25 (m, 4H), 3.10 (m, 2H), 2.95 (m, 2H).

Example 33 1-Cyclobutyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline 2,2,2-trifluoroacetate (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-433 of Table A) 33.1 Preparation of tert-butyl 1-cyclobutyl-2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate

A solution of 79 mg (0.237 mmol) of tert-butyl 2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate (from step 32.2) in 2 ml THF was treated with 38.3 mg (0.546 mmol) of cyclobutanone and molecular sieves (4 Å). The reaction mixture was stirred at room temperature overnight. 231 mg (1.09 mmol) of sodium triacetoxyborohydride was added and the reaction mixture was stirred overnight at room temperature. The reaction mixture was diluted with ethyl acetate and extracted once with a 1 molar aqueous solution of sodium hydroxide. The organic phase was dried with magnesium sulfate, concentrated in vacuo and the residue was purified by column chromatography on silica (eluent: 0-10% methanol in dichloromethane) yielding 78 mg (0.205 mmol) of the title compound.

ESI-MS [M+H⁺]=344.20

33.2 Preparation of 1-cyclobutyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline 2,2,2-trifluoroacetate

78.4 mg (0.228 mmol) of tert-butyl 1-cyclobutyl-2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate (from step 33.1) were dissolved in 1 ml of dichloromethane and treated with 0.53 ml (6.85 mmol) of trifluoroacetic acid at 0° C. The solution was stirred for 2 h and then concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-30% methanol in dichloromethane) to yield 69 mg of crude product, which was purified again via preparative HPLC to yield 46 mg of the title compound.

ESI-MS [M+H⁺]=244.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 8.70 (bs, 2H), 6.80 (m, 1H), 6.75 (d, 1H), 6.70 (d, 1H), 4.10 (m, 2H), 4.05 (m, 1H), 3.25 (m, 2H), 3.20 (m, 2H), 3.10 (m, 4H), 2.20 (m, 2H), 2.10 (m, 2H), 1.65 (m, 2H).

Example 34 1-Methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.a, I.b or I.c in which the Combination of R⁵, R^(5b), R⁶ and R^(9a) is as in row A-253 of Table A)

The title compound was prepared in analogy to example 33, using however formaldehyde instead of cyclobutanone.

ESI-MS [M+H⁺]=204.10

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.85 (m, 1H), 6.65 (d, 1H), 6.55 (d, 1H), 3.90 (s, 2H), 3.35 (m, 2H), 3.15 (m, 2H), 3.10 (m, 2H), 2.95 (m, 5H).

Example 35 1-(Oxetan-3-yl)-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline 2,2,2-trifluoroacetate (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in row A-541 of Table A)

The title compound was prepared in analogy to example 33, using however oxetan-3-one instead of cyclobutanone.

ESI-MS [M+H⁺]=246.15

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 8.80 (m, 2H), 6.75 (m, 2H), 6.30 (d, 1H), 4.80 (m, 2H), 4.65 (m, 3H), 4.10 (s, 2H), 3.35 (m, 2H), 3.20 (m, 4H), 3.10 (m, 2H).

Example 36 1-(Cyclopropylmethyl)-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-577 of Table A)

The title compound was prepared in analogy to example 33, using however cyclopropanecarboxaldehyde instead of cyclobutanone.

ESI-MS [M+H⁺]=244.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.85 (m, 1H), 6.75 (m, 1H), 6.55 (m, 1H), 4.00 (m, 2H), 3.35-3.15 (m, 8H), 3.00 (m, 2H), 1.05 (m, 1H), 0.50 (m, 2H), 0.20 (m, 2H).

Example 37 1-(Cyclopentylmethyl)-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-649 of Table A)

The title compound was prepared in analogy to example 33, using however cyclopentanecarboxaldehyde instead of cyclobutanone.

ESI-MS [M+H⁺]=272.20

¹H NMR (DMSO-d⁶, 500 MHz): δ[ppm]: 6.80 (m, 1H), 6.65 (d, 1H), 6.50 (d, 1H), 3.95 (m, 2H), 3.30-3.20 (m, 6H), 3.15 (m, 2H), 2.95 (m, 2H), 2.30 (m, 1H), 1.90-1.55 (m, 6H), 1.25 (m, 2H).

Example 38 Cyclopropyl(2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxalin-1-yl)methanone (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-721 of Table A) 38.1 Preparation of tert-butyl 1-(cyclopropanecarbonyl)-2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate

To 50 mg (0.173 mmol) of tert-butyl 2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate dissolved in 1 ml of dichloromethane were added 0.77 ml (4.43 mmol) of N,N-diisopropylethylamine in an inert atmosphere at 0° C. 19 μl (0.21 mmol) of cyclopropanecarbonyl chloride was dissolved in 1 ml of dichloromethane and slowly added to the reaction mixture. The reaction mixture was stirred at room temperature for 5 h. The solution was diluted with dichloromethane and treated twice with 10% aqueous solution of citric acid. The organic phase was washed once with saturated sodium chloride solution, dried with MgSO₄ and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-10% methanol in dichloromethane) yielding 35 mg (0.098 mmol) of the title compound.

ESI-MS [M-tert-butyl+H⁺]=302.10

38.2 Preparation of cyclopropyl(2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]-quinoxalin-1-yl)methanone

35 mg (0.098 mmol) of tert-butyl 1-(cyclopropanecarbonyl)-2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate were dissolved in 2 ml of dichloromethane and treated with 150 μl (1.96 mmol) of trifluoroacetic acid at 0° C. The solution was stirred overnight at room temperature. 100 μl (1.31 mmol) of trifluoroacetic acid were added and the reaction mixture was stirred for 1 h. The reaction mixture was treated 3× with acidified water. The combined aqueous phase was basified with 1 N sodium hydroxide solution and extracted 5× with dichloromethane. The combined organic phase was dried with MgSO₄ and concentrated in vacuo to yield 23 mg of the title compound.

ESI-MS [M+H⁺]=258.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 7.30 (m, 1H), 7.05 (m, 1H), 6.80 (m, 1H), 4.10 (s, 2H), 3.90 (m, 2H), 3.45 (m, 4H), 3.30 (m, 2H), 2.10 (m, 1H), 1.15 (m, 2H), 0.85 (m, 2H).

Example 39 Cyclopentyl(2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxalin-1-yl)methanone (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in row A-793 of Table A)

The title compound was prepared in analogy to example 38 using cyclopentanecarbonyl chloride.

ESI-MS [M+H⁺]=286.20 ¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 7.00 (m, 2H), 6.80 (m, 1H), 4.10 (s, 2H), 3.90 (m, 2H), 3.45-3.20 (m, 7H), 1.80 (m, 6H), 1.55 (m, 2H).

Example 40 1-Cyclopropyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-397 of Table A) 40.1 Preparation of 2-(4-cyclopropyl-3,4-dihydroquinoxalin-1(2H)-yl)acetamide

A solution of 500 mg (2.87 mmol) of 1-cyclopropyl-1,2,3,4-tetrahydroquinoxaline in 5 ml dimethylformamide was treated with 2.0 ml (11.68 mmol) of N-ethyl-N-isopropylpropan-2-amine, and subsequently 555 mg (5.94 mmol) 2-chloroacetamide were added. The reaction mixture was heated in a microwave system at 100° C. for 12 hours. The reaction mixture was quenched with water and basified with 1 N sodium hydroxide solution. The aqueous phase was extracted 3× with dichloromethane. The combined organic extracts were dried with magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-20% methanol in dichloromethane) to yield 620 mg of the title compound.

ESI-MS [M+H⁺]=232.20

40.2 Preparation of 2-(4-cyclopropyl-3,4-dihydroquinoxalin-1(2H)-yl)ethanamine

To 620 mg (2.68 mmol) of 2-(4-cyclopropyl-3,4-dihydroquinoxalin-1 (2H)-yl)acetamide in 2 ml of THF was added 5.4 ml (10.80 mmol) of 2 molar borane dimethylsulfide THF solution and subsequently heated for 7 hours at 60° C. in a microwave system. An additional 2.7 ml (5.40 mmol) of 2 molar borane dimethylsulfide THF solution was added to the reaction mixture and heated for 10 hours at 60° C. in a microwave system. To the reaction mixture were added 2 ml of methanol, acidified with 2 molar hydrochloric acid and heated for 15 minutes at 60° C. in a microwave system. The reaction mixture was diluted with ethyl acetate and extracted twice with 1 molar hydrochloric acid. The combined aqueous phases were set to pH 10 with sodium hydroxide solution and extracted 3× with dichloromethane. The combined organic phases were dried and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-15% methanol in dichloromethane) to yield 347 mg of the title compound.

ESI-MS [M+^(H)]=218.20

40.3 Preparation of 1-Cyclopropyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]-quinoxaline

A solution of 347 mg (1.6 mmol) of 2-(4-cyclopropyl-3,4-dihydroquinoxalin-1(2H)-yl)ethanamine in 5 ml of ethanol were treated with 119 μl (1.6 mmol) of 37% aqueous formaldehyde solution and 135 μl (1.76 mmol) of trifluoroacetic acid. The reaction mixture was stirred for 36 h at room temperature. Water was added and the reaction mixture was basified using 2 N aqueous sodium hydroxide solution. The aqueous phase was extracted three times with dichloromethane. The combined organic phases were dried and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-20% methanol in dichloromethane) to yield 177 mg of the title compound.

ESI-MS [M+H⁺]=230.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 7.10 (d, 1H), 6.80 (m, 1H), 6.60 (d, 1H), 3.85 (s, 2H), 3.20 (m, 2H), 3.10 (m, 2H), 3.00 (m, 4H), 2.25 (m, 1H), 0.80 (m, 2H), 0.55 (m, 2H).

Example 41 1-Cyclopentyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5b), R^(5b), R⁶ and R^(9a) is as in Row A-469 of Table A)

The title compound was prepared in analogy to example 40 using 1-cyclopentyl-1,2,3,4-tetrahydroquinoxaline as starting material.

ESI-MS [M+H⁺]=258.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.80 (d, 1H), 6.70 (m, 1H), 6.45 (d, 1H), 4.25 (m, 1H), 3.75 (s, 2H), 3.15 (m, 2H), 3.05 (m, 2H), 2.90 (m, 2H), 2.85 (m, 2H), 1.80 (m, 2H), 1.65 (m, 2H), 1.55 (m, 4H).

Example 42 1-Cyclopropyl-5-methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.gg, I.hh or I.ii in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-397 of Table A) 42.1 Preparation of 2-(4-cyclopropyl-3,4-dihydroquinoxalin-1 (2H)-yl)propanamide

A solution of 300 mg (1.72 mmol) of 1-cyclopropyl-1,2,3,4-tetrahydroquinoxaline in 3 ml dimethylformamide was treated with 1.2 ml (7.0 mmol) of N-ethyl-N-isopropylpropan-2-amine, 387 mg (2.58 mmol) of sodium iodide and subsequently 523 mg (3.44 mmol) of 2-bromopropanamide were added. The reaction mixture was heated in a microwave system at 100° C. for 8 hours. The reaction mixture was quenched with water and basified with 1 N sodium hydroxide solution. The aqueous phase was extracted 3× with dichloromethane. The combined organic extracts were dried with magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-20% methanol in dichloromethane) to yield 453 mg of the title compound.

ESI-MS [M+H⁺]=246.20

42.2 Preparation of 2-(4-cyclopropyl-3,4-dihydroquinoxalin-1(2H)-yl)propan-1-amine

To 453 mg (1.85 mmol) of 2-(4-cyclopropyl-3,4-dihydroquinoxalin-1(2H)-yl)propanamide in 2 ml THF were added 4.3 ml (8.60 mmol) of 2 molar borane dimethylsulfide THF solution and subsequently heated for 9 hours at 60° C. and 2 hours at 70° C. in a microwave system. To the reaction mixture was added 2 ml of methanol, acidified with 2 molar hydrochloric acid and heated for 15 minutes at 60° C. in a microwave system. The reaction mixture was diluted with ethyl acetate and extracted twice with 1 molar hydrochloric acid. The combined aqueous phases were set to pH 10 with sodium hydroxide solution and extracted 3× with dichloromethane. The combined organic phases were dried and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-15% methanol in dichloromethane) to yield 209 mg of the title compound.

ESI-MS [M+H⁺]=232.20

42.3 Preparation of 1-cyclopropyl-5-methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino-[1,7,6-de]quinoxaline

A solution of 209 mg (0.9 mmol) of 2-(4-cyclopropyl-3,4-dihydroquinoxalin-1(2H)-yl)propan-1-amine in 3 ml of ethanol were treated with 67 μl (0.9 mmol) of 37% aqueous formaldehyde solution and 76 μl (0.99 mmol) of trifluoroacetic acid. The reaction mixture was stirred for 36 h at room temperature. Water was added and the reaction mixture was basified using 2 N aqueous sodium hydroxide solution. The aqueous phase was extracted three times with dichloromethane. The combined organic phases were dried and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-20% methanol in dichloromethane) to yield 136 mg of the title compound.

ESI-MS [M+H⁺]=244.20

1H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 7.00 (d, 1H), 6.65 (m, 1H), 6.50 (d, 1H), 3.75 (d, 1H), 3.45 (d, 1H), 3.30-3.15 (m, 4H), 3.05 (m, 1H), 2.80 (d, 1H), 2.65 (d, 1H), 2.20 (m, 1H), 0.90 (d, 3H), 0.80 (m, 2H), 0.50 (m, 2H).

Example 43 1-Cyclopentyl-5-methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.gg, I.hh or I.ii in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-469 of Table A)

The title compound was prepared in analogy to example using however 1-cyclopentyl-1,2,3,4-tetrahydroquinoxaline instead of 1-cyclopropyl-1,2,3,4-tetrahydroquinoxaline.

ESI-MS [M+H⁺]=272.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.70 (d, 1H), 6.65 (m, 1H), 6.40 (d, 1H), 4.20 (m, 1H), 3.75 (d, 1H), 3.50 (d, 1H), 3.25-3.10 (m, 3H), 3.00 (m, 2H), 2.85 (d, 1H), 2.70 (d, 1H), 1.80 (m, 2H), 1.70-1.55 (m, 5H), 1.50 (m, 1H), 0.90 (d, 3H).

Example 44

5,6,7,9,9a,10,11,12,13,14-decahydro-4H-azepino[1,2-a][1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-937 of Table A)

44.1 Preparation of ethyl 1-(2-nitrophenyl)azepane-2-carboxylate

A solution of 450 mg (3.19 mmol) of 1-fluoro-2-nitrobenzene, 546 mg (3.19 mmol) of ethyl azepane-2-carboxylate and 0.89 ml (6.38 mmol) of triethylamine in 10 ml acetonitrile was stirred overnight at reflux. The reaction mixture was concentrated in vacuo. To the residue was added aqueous sodium bicarbonate solution and extracted twice with ethyl acetate. The combined organic extracts were dried with sodium sulfate and concentrated in vacuo to yield 780 mg of the crude title compound. The crude product was used without further purification in the next step.

ESI-MS [M+H⁺]=293.10

44.2 Preparation of 6a,7,8,9,10,11-hexahydroazepino[1,2-a]quinoxalin-6(5H)-one

780 mg (2.67 mmol) of ethyl 1-(2-nitrophenyl)azepane-2-carboxylate were dissolved in 30 ml methanol and treated with 284 mg of 10% Pd/C in a hydrogen atmosphere. The solution was stirred at room temperature for 1 h. The catalyst was filtered off and the solution was concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-50% ethyl acetate in heptane) to yield 159 mg of the title compound.

ESI-MS [M+H⁺]=217.10

44.3 Preparation of 5,6,6a,7,8,9,10,11-octahydroazepino[1,2-a]quinoxaline

To 105 mg (0.485 mmol) 6a,7,8,9,10,11-hexahydroazepino[1,2-a]quinoxalin-6(5H)-one in 4 ml of THF (tetrahydrofuran) were added 0.97 ml (0.97 mmol) of 1 molar borane dimethylsulfide THF solution and subsequently heated for 1 h at 80° C. in a microwave system. The reaction mixture was poured on ice water, acidified with hydrochloric acid solution to pH=5 and extracted twice with ethyl acetate. The combined organic phases were dried and concentrated in vacuo. The residue was acidified with hydrochloric acid solution and extracted once with ether. The aqueous phase was basified with aqueous sodium bicarbonate solution and extracted 3× with dichloromethane. The combined organic phases were dried and concentrated in vacuo to yield 85 mg of the crude title compound.

ESI-MS [M+H⁺]=203.20

44.4 Preparation of 2-(6a,7,8,9,10,11-hexahydroazepino[1,2-a]quinoxalin-5(6H)-yl)-acetamide

A solution of 85 mg (0.40 mmol) of 5,6,6a,7,8,9,10,11-octahydroazepino[1,2-a]quinoxaline in 2 ml of dimethylformamide was treated with 16 mg (0.40 mmol) of sodium hydride (60% in mineral oil) and stirred for 15 min at room temperature. 112 mg (1.2 mmol) of 2-chloroacetamide were added and the reaction mixture was heated in a microwave system at 100° C. for 4 hours. 209 μl (1.2 mmol) of N-ethyl-N-isopropylpropan-2-amine were added to the reaction mixture and heated at 100° C. for 2 hours. 110 mg (0.8 mmol) of 2-bromoacetamide were added and the reaction mixture was heated in a microwave system at 100° C. for 2 hours. The reaction mixture was basified with sodium bicarbonate solution and extracted 2× with ethyl acetate. The combined organic extracts were dried with magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-50% ethyl acetate in heptane) to yield 42 mg of the title compound.

ESI-MS [M+H⁺]=260.20

44.5 Preparation of 2-(6a,7,8,9,10,11-hexahydroazepino[1,2-a]quinoxalin-5(6H)-yl)-ethanamine

To 42 mg (0.146 mmol) of 2-(6a,7,8,9,10,11-hexahydroazepino[1,2-a]quinoxalin-5(6H)-yl)acetamide in 1 ml of THF were added 292 μl (8.60 mmol) of 2 molar borane dimethylsulfide THF solution and subsequently heated for 6 hours at 60° C. in a microwave system. Additional 292 μl (8.60 mmol) of 2 molar borane dimethylsulfide THF solution were added to the reaction mixture and heated for 4 hours at 60° C. in a microwave system. To the reaction mixture was added 2 ml of methanol, acidified with 2 molar aqueous hydrochloric acid solution and heated for 15 minutes at 60° C. in a microwave system. The reaction mixture was diluted with ethyl acetate and extracted twice with 1 molar hydrochloric acid. The combined aqueous phases were set to pH 10 with sodium hydroxide solution and extracted 3× with dichloromethane. The combined organic phases were dried and concentrated in vacuo to yield 36 mg of the title compound.

ESI-MS [M+H⁺]=246.20

44.6 Preparation of 5,6,7,9,9a,10,11,12,13,14-decahydro-4H-azepino[1,2-a][1,4]-diazepino[1,7,6-de]quinoxaline

A solution of 36 mg (0.147 mmol) of 2-(6a,7,8,9,10,11-hexahydroazepino[1,2-a]quinoxalin-5(6H)-yl)ethanamine in 2 ml of ethanol were treated with 11 μl (0.147 mmol) of 37% aqueous formaldehyde solution and 12 μl (0.161 mmol) of trifluoroacetic acid. The reaction mixture was stirred overnight at room temperature. The reaction mixture was concentrated in vacuo, treated with aqueous sodium bicarbonate solution and extracted twice with dichloromethane. The combined organic phases were dried and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-20% methanol in dichloromethane) to yield 12.7 mg of the title compound.

ESI-MS [M+H⁺]=258.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.65 (m, 1H), 6.50 (d, 1H), 6.35 (d, 1H), 3.70 (m, 1H), 3.60 (m, 1H), 3.20 (m, 2H), 3.10 (m, 1H), 3.00 (m, 3H), 2.95 (m, 1H), 2.85 (m, 1H), 2.80 (m, 1H), 1.80 (m, 2H), 1.65-1.50 (m, 4H), 1.40 (m, 2H).

Example 45 7-Methyl-5,6,7,9,9^(a), 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (Compound of the Formula I.gg, I.hh or I.ii in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-865 of Table A)

The title compound was prepared in analogy to example 42, using however 1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoxaline and 2-bromopropanamide.

ESI-MS [M+H⁺]=244.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.80 (m, 1H), 6.50 (d, 1H), 6.45 (d, 1H), 3.95 (d, 1H), 3.70 (d, 1H), 3.50 (m, 2H), 3.15 (m, 2H), 2.85 (m, 2H), 2.75 (m, 1H), 2.20 (m, 1H), 2.10 (m, 1H), 2.00 (m, 1H), 1.90 (m, 1H), 1.35 (m, 1H), 1.20 (d, 3H).

Example 46 1-Fluoro-7-methyl-5,6,7,9,9^(a),10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (Compound of the Formula I.gg in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-866 of Table A)

The title compound was prepared in analogy to example 42, using however 9-fluoro-1,2,3,3a,4,5-hexahydropyrrolo[1,2-a]quinoxaline and 2-bromopropanamide.

ESI-MS [M+H⁺]=262.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.60 (m, 1H), 6.55 (m, 1H), 3.90 (d, 1H), 3.80 (m, 1H), 3.55 (d, 1H), 3.20 (d, 1H), 3.00 (m, 2H), 2.80 (m, 2H), 2.55 (m, 1H), 2.15 (m, 2H), 1.80 (m, 2H), 1.50 (m, 1H), 1.25 (d, 3H).

Example 47 1,2,3,4,6,7-Hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopropane](Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-281 of Table B) 47.1 Preparation of 2-(2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-quinolin]-1′-yl)-acetamide

A solution of 500 mg (3.14 mmol) of 2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-quinoline] in 5 ml of dimethylformamide was treated with 2.2 ml (12.8 mmol) of N-ethyl-N-isopropylpropan-2-amine and 706 mg (4.71 mmol) of sodium iodide; and subsequently 670 mg (7.16 mmol) of 2-chloroacetamide were added. The reaction mixture was heated in a microwave system at 100° C. for 10 hours. The reaction mixture was quenched with water and basified with 1 N sodium hydroxide solution. The aqueous phase was extracted 3× with dichloromethane. The combined organic extracts were dried with magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-20% methanol in dichloromethane) to yield 624 mg of the title compound.

ESI-MS [M+H⁺]=217.20

47.2 Preparation of 2-(2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-quinolin]-1′-yl)ethan-amine

To 624 mg (2.89 mmol) of 2-(2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-quinolin]-1′-yl)acetamide in 2 ml of THF were added 5.77 ml (11.54 mmol) of 2 molar borane dimethylsulfide THF solution and subsequently heated for 9 hours at 60° C. in a microwave system. To the reaction mixture were added 2 ml of methanol, acidified with 2 molar hydrochloric acid and heated for 15 minutes at 60° C. in a microwave system. The reaction mixture was diluted with ethyl acetate and extracted twice with 1 molar hydrochloric acid. The combined aqueous phases were set to pH 10 with sodium hydroxide solution and extracted 3× with dichloromethane. The combined organic phases were dried and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-20% methanol in dichloromethane) to yield 299 mg of the title compound.

ESI-MS [M+H⁺]=203.20

47.3 Preparation of 1,2,3,4,6,7-Hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopropane]

A solution of 299.6 mg (1.48 mmol) of 2-(2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-quinolin]-1′-yl)ethanamine in 3 ml of ethanol was treated with 110 μl (1.48 mmol) of 37% aqueous formaldehyde solution and 126 μl (1.63 mmol) of trifluoroacetic acid. The reaction mixture was stirred overnight at room temperature. Water was added and the reaction mixture was basified using 2 N aqueous sodium hydroxide solution. The aqueous phase was extracted three times with dichloromethane. The combined organic phases were dried and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-20% methanol in dichloromethane) to yield 131 mg of the title compound.

ESI-MS [M+H⁺]=215.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.90 (d, 1H), 6.70 (m, 1H), 6.55 (d, 1H), 3.75 (s, 2H), 3.25 (m, 2H), 3.00 (m, 2H), 2.90 (m, 2H), 1.60 (m, 2H), 0.95 (s, 2H), 0.80 (s, 2H).

Example 48 4-Methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopropane](Compound of the Formula I.s, I.t or I.u in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in row B-281 of Table B)

The title compound was prepared in analogy to example 47, using however 2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-quinoline] and 2-bromopropanamide.

ESI-MS [M+H⁺]=229.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.85 (d, 1H), 6.65 (m, 1H), 6.55 (d, 1H), 3.80 (d, 1H), 3.50 (d, 1H), 3.25 (m, 3H), 2.85 (d, 1H), 2.70 (d, 1H), 1.70 (m, 1H), 1.60 (m, 1H), 1.05 (m, 1H), 0.90 (m, 3H), 0.85 (m, 1H), 0.75 (m, 2H).

Example 49 11-Fluoro-8,8-Dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (Compound of the Formula I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in row B-2 of Table B)

The title compound was prepared in analogy to example 47, using however 7-fluoro-4,4-dimethyl-1,2,3,4-tetrahydroquinoline and 2-bromoacetamide.

ESI-MS [M+H⁺]=235.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 7.15 (dd, 1H), 6.55 (dd, 1H), 3.80 (s, 2H), 3.20 (m, 2H), 3.10 (m, 2H), 2.90 (m, 2H), 1.60 (m, 2H), 1.20 (s, 6H).

Example 50 10-Methoxy-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline, trifluoroacetic acid (Compound of the Formula I.h in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in row B-7 of Table B)

The title compound was prepared in analogy to example 1, using however 7-methoxy-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate and 3-methylbut-2-enoyl chloride.

ESI-MS [M+H⁺]=247.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 8.75 (bs, 2H), 6.95 (s, 1H), 6.85 (s, 1H), 4.15 (m, 2H), 3.70 (s, 3H), 3.20 (m, 2H), 3.15 (m, 4H), 1.65 (m, 2H), 1.25 (s, 6H).

Example 51 4,8,8-Trimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline 2,2,2-trifluoroacetate (Compound of the Formula I.s, I.t or I.u in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in row B-1 of Table B)

The title compound was prepared in analogy to example 47, using however 4,4-dimethyl-1,2,3,4-tetrahydroquinoline and 2-bromopropanamide.

ESI-MS [M+H⁺]=231.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 9.90 (bs, 1H), 9.20 (bs, 1H); 7.35 (d, 1H), 7.10 (d, 1H), 6.90 (m, 1H), 4.30 (d, 1H), 4.05 (d, 1H), 3.45 (m, 1H), 3.25 (m, 3H), 3.15 (m, 1H), 1.70 (m, 2H), 1.30 (m, 9H).

Example 52 4-Ethyl-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (Compound of the Formula I.v, I.w or I.x in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-1 of Table B)

The title compound was prepared in analogy to example 47, using however 4,4-dimethyl-1,2,3,4-tetrahydroquinoline and 2-bromobutanamide.

ESI-MS [M+H⁺]=245.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 7.15 (d, 1H), 6.85 (d, 1H), 6.70 (m, 1H), 3.85 (d, 1H), 3.50 (d, 1H), 3.20 (m, 2H), 3.00 (d, 1H), 2.95 (m, 1H), 2.75 (d, 1H), 1.60 (m, 2H), 1.40 (m, 2H), 1.25 (s, 3H), 1.30 (s, 3H), 0.80 (m, 3H).

Example 53 6,8,8-Trimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline (Compound of the Formula I.y, I.z or I.Zz in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-1 of Table B)

The title compound was prepared in analogy to example 47, using however 2,4,4-trimethyl-1,2,3,4-tetrahydroquinoline and 2-chloroacetamide.

ESI-MS [M+H⁺]=231.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 7.05 (d, 1H), 6.90 (d, 1H), 6.65 (m, 1H), 3.85 (d, 1H), 3.45 (d, 1H), 3.30 (m, 3H), 3.00 (m, 1H), 2.70 (m, 1H), 1.65 (m, 1H), 1.40 (m, 1H), 1.25 (s, 3H), 1.15 (s, 6H).

Example 54 One Enantiomer of 8-ethyl-8-methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]-quinoline, Trifluoroacetic Acid (Enantiomer of the Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-41 of Table B)

The title compound was prepared in analogy to example 1, using however tert-butyl 2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate and (Z)-3-methylpent-2-enoyl chloride.

ESI-MS [M+H⁺]=231.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 8.90 (bs, 1H), 8.65 (bs, 1H), 7.30 (d, 1H), 7.15 (d, 1H), 6.90 (m, 1H), 4.20 (m, 1H), 4.10 (m, 1H), 3.25 (m, 6H), 1.85 (m, 1H), 1.70 (m, 1H), 1.60 (m, 1H), 1.45 (m, 1H), 1.20 (s, 3H), 0.70 (m, 3H).

Example 55 Other enantiomer of 8-ethyl-8-methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline, Trifluoroacetic Acid (Enantiomer of the Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in row B-41 of Table B)

The title compound was prepared in analogy to example 1, using however tert-butyl 2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate and (Z)-3-methylpent-2-enoyl chloride.

ESI-MS [M+H⁺]=231.10

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 8.90 (bs, 1H), 8.65 (bs, 1H), 7.30 (d, 1H), 7.15 (d, 1H), 6.90 (m, 1H), 4.20 (m, 1H), 4.10 (m, 1H), 3.20 (m, 6H), 1.85 (m, 1H), 1.70 (m, 1H), 1.60 (m, 1H), 1.45 (m, 1H), 1.20 (s, 3H), 0.70 (m, 3H).

Example 56 4-Methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane](Compound of the Formula I.s, I.t or I.u in which the Combination of R^(5a), R^(5b), R, R⁸ and R^(9a) is as in row B-321 of Table B) 56.1 Preparation of 2-cyclobutylidene-N-phenylacetamide

3.35 g (36 mmol) of aniline were dissolved in 60 ml of dichloromethane and treated with 13.83 ml (79 mmol) of N-ethyl-N-isopropylpropan-2-amine. Within 10 min 19.80 ml of a 1 molar solution of 2-cyclobutylideneacetyl chloride in dichloromethane was added at 0° C. and the solution was stirred overnight at room temperature. The reaction mixture was poured on ice water and extracted 2× with dichloromethane. The combined organic phases were washed once with saturated sodium chloride solution, dried with magnesium sulfate and concentrated in vacuo. The crude oil was dissolved in dichloromethane and treated with ether till crystallization, yielding 5.5 g of the title compound.

ESI-MS [M+H⁺]=188.10

56.2 Preparation of 1′H-spiro[cyclobutane-1,4′-quinolin]-2′(3′H)-one

A solution of 2.0 g (10.68 mmol) of 2-cyclobutylidene-N-phenylacetamide in 214 ml of toluene was irradiated with a 700 W mercury lamp in a flow reactor (FEP-tubing, pyrex filter) with a flow rate of 1 ml per min at a temperature range of 0° C. to 20° C. with a residence time of 5 to 7 min. The reaction mixture was concentrated in vacuo and the residue was purified by column chromatography on silica (eluent: 0-55% ethyl acetate in cyclohexane) to yield 940 mg of the title compound.

ESI-MS [M+H⁺]=188.10

56.3 Preparation of 2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinoline]

To 850 mg (4.54 mmol) of 1′H-spiro[cyclobutane-1,4′-quinolin]-2′(3′H)-one in 5 ml of THF were added 9.08 ml (9.08 mmol) of 1 molar borane dimethylsulfide THF solution and subsequently heated for 30 min at 80° C. in a microwave system. The reaction mixture was acidified with 6 molar hydrochloric acid solution and treated with ethyl acetate. The organic phase was extracted twice with 1 molar hydrochloric acid solution. The combined aqueous phases were set to pH 10 with sodium bicarbonate and extracted 3× with ethyl acetate. The combined organic phases were dried and concentrated in vacuo to yield 565 mg of the crude title compound.

ESI-MS [M+H⁺]=174.10

56.4 Preparation of 2-(2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinolin]-1′-yl)propanamide

ESI-MS [M+H⁺]=245.20

A solution of 300 mg (1.73 mmol) of 2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinoline] in 10 ml dimethylformamide was treated with 69 mg (1.73 mmol) of sodium hydride (60% in mineral oil) and stirred for 15 min at 50° C., then transferred to a microwave vial and stirred for 5 min at 70° C. in a microwave system. Subsequently 790 mg (5.19 mmol) of 2-bromoacetamide were added and the reaction mixture was heated in a microwave system at 100° C. for 7 hours. Additional 263 mg (1.73 mmol) of 2-bromoacetamide were added and the reaction mixture was heated in a microwave system at 100° C. for 2 hours. The reaction mixture was quenched with ice water, acidified to pH=5 and extracted with ether. The aqueous phase was basified with sodium bicarbonate solution and extracted 3× with dichloromethane. The combined organic extracts were dried with magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-55% ethyl acetate in heptane) to yield 258 mg of the title compound.

56.5 Preparation of 2-(2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinolin]-1′-yl)propan-1-amine

To 258 mg (0.348 mmol) of 2-(2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinolin]-1′-yl)propanamide in 2 ml THF were added 1.05 ml (2.10 mmol) of 2 molar borane dimethylsulfide THF solution and subsequently heated for 6 hours at 60° C. in a microwave system. Subsequently 348 μl (0.70 mmol) of 2 molar borane dimethylsulfide THF solution was added to the reaction mixture and heated for 2 hours at 60° C. in a microwave system. Subsequently 697 μl (1.39 mmol) of 2 molar borane dimethylsulfide THF solution was added to the reaction mixture and heated for 3 hours at 60° C. in a microwave system. To the reaction mixture was added 2 ml of methanol, acidified with 2 molar hydrochloric acid and heated for 5 minutes at 60° C. in a microwave system. The reaction mixture was diluted with ethyl acetate and extracted twice with 1 molar hydrochloric acid. The combined aqueous phases were set to pH 10 with sodium bicarbonate solution and extracted 3× with dichloromethane. The combined organic phases were dried and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-20% methanol in dichloromethane) to yield 90 mg of the title compound.

ESI-MS [M+H⁺]=231.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 7.35 (d, 1H), 6.95 (dd, 1H), 6.70 (d, 1H), 6.55 (dd, 1H), 3.80 (m, 1H), 3.05 (m, 1H), 3.00 (m, 1H), 2.70 (m, 1H), 2.55 (m, 1H), 2.35 (m, 1H), 2.25 (m, 1H), 2.00 (m, 1H), 1.90 (m, 5H), 1.05 (d, 3H).

56.6 Preparation of 4-methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]-quinoline-8,1′-cyclobutane]

A solution of 90 mg (0.313 mmol) of 2-(2′,3′-dihydro-1′H-spiro[cyclobutane-1,4′-quinolin]-1′-yl)propan-1-amine in 2 ml of ethanol was treated with 23 μl (0.313 mmol) of 37% aqueous formaldehyde solution and 26 μl (0.344 mmol) of trifluoroacetic acid. The reaction mixture was stirred overnight at room temperature. Further 12 μl (0.156 mmol) of 37% aqueous formaldehyde solution and 12 μl (0.156 mmol) of trifluoroacetic acid were added to the reaction mixture and stirring was continued overnight at room temperature. The reaction mixture was concentrated in vacuo and to the residue was added aqueous sodium bicarbonate solution. The aqueous phase was extracted twice with dichloromethane. The combined organic phases were dried and concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-10% methanol in dichloromethane) to yield 38 mg of the title compound.

ESI-MS [M+H⁺]=243.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 7.35 (d, 1H), 6.90 (d, 1H), 6.75 (d, 1H), 3.80 (m, 1H), 3.40 (m, 1H), 3.20 (m, 2H), 3.10 (m, 1H), 2.80 (m, 1H), 2.70 (m, 1H), 2.40 (m, 1H), 2.15 (m, 1H), 2.00 (m, 4H), 1.85 (m, 1H), 1.70 (m, 1H), 0.80 (s, 3H).

Example 57 1-Fluoro-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline, Trifluoroacetic Acid (Compound of the Formula I.a in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-866 of Table A) 57.1 Preparation of methyl pyrrolidine-2-carboxylate

To a solution of pyrrolidine-2-carboxylic acid (75 g, 651 mmol) in methanol (750 ml), SOCl₂ (250 ml) was added dropwise at 0° C., and the reaction mixture was stirred for 16 hrs at 20° C. One additional vial was set up in the same way. Both reaction mixtures were combined and concentrated under reduced pressure to give the title compound (90 g, 543 mmol, yield 50%).

¹H NMR (400 MHz, DMSO-d₆): δ[ppm]: 9.83 (s, 1H), 4.32 (t, J=7.6 Hz, 1H), 3.72 (s, 3H), 3.21-3.15 (m, 2H), 2.22-2.20 (m, 1H), 1.96-1.87 (m, 3H)

57.2 Preparation of methyl 1-(2-fluoro-6-nitro-phenyl)-pyrrolidine-2-carboxylate

To a mixture of methyl pyrrolidine-2-carboxylate (17.18 g, 104 mmol) in acetonitril (500 mL), triethylamine (26.3 mL, 189 mmol) and 1,2-difluoro-3-nitrobenzene (15 g, 94 mmol) were added at 20° C., and the reaction mixture was stirred for 12 h at 80° C. Then the mixture was cooled to 20° C., concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (petrol ether:ethyl acetate=20:1 to 10:1) to give the title compound (20 g, 74.6 mmol, yield 79%).

¹H NMR (400 MHz, CDCl₃): δ[ppm]: 7.36 (d, J=8 Hz, 1H), 7.15-7.11 (m, 1H), 6.99-6.96 (m, 1H), 4.35-4.31 (m, 1H), 3.55 (s, 3H), 3.52-3.49 (m, 1H), 3.06-3.04 (m, 1H), 2.29-2.26 (m, 1H), 2.06-1.89 (m, 3H)

57.3 Preparation of 9-fluoro-2,3,3a,5,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-4-one

To a solution of methyl 1-(2-fluoro-6-nitro-phenyl)-pyrrolidine-2-carboxylate (10 g, 37.3 mmol) in methanol (200 ml), Pd/C (3.97 g, 37.3 mmol) was added under Ar protection, then the reaction mixture was stirred for 12 h at 20° C. at 15 psi under H₂ atmosphere. One additional vial was set up as described above. The two reaction mixtures were combined, filtered, and the filtrate was concentrated under reduced pressure to give the title compound (10 g, 48.5 mmol, yield 65%).

¹H NMR (400 MHz, CDCl₃): δ[ppm]: 9.33 (s, 1H), 6.73-6.63 (m, 2H), 6.55-6.53 (m, 1H), 3.89-3.86 (m, 1H), 3.72-3.68 (m, 1H), 3.40-3.39 (m, 1H), 2.30-2.22 (m, 2H), 1.92-1.84 (m, 2H)

57.4 Preparation of 9-fluoro-1,2,3,3a,4,5,5a,6-octahydropyrrolo[1,2-a]quinoxaline

To a solution of 9-fluoro-2,3,3a,5,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-4-one (10 g, 48.5 mmol) in THF (200 ml), a solution of BH₃.THF (12.5 g, 145 mmol) was added at 0° C., then the reaction solution was stirred 12 h at 70° C. After cooling to 0° C., methanol (100 ml) was added dropwise at 0° C., and the reaction solution was stirred for 30 minutes at 20° C., concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (petrol ether:ethyl acetate=20:1 to 10:1) to give the title compound (5 g, 26 mmol, yield 53.6%).

¹H NMR (400 MHz, CDCl₃): δ[ppm]: 6.54-6.49 (m, 1H), 6.40-6.37 (m, 1H), 6.28 (d, J=8 Hz, 1H), 3.92 (s, 1H), 3.78-3.76 (m, 1H), 3.34-3.20 (m, 1H), 3.20-3.17 (m, 1H), 2.99-2.97 (m, 1H), 2.66-2.61 (m, 1H), 2.13-2.11 (m, 1H), 1.86-1.78 (m, 2H), 1.50-1.47 (m, 1H)

57.5 Preparation of 2-(9-fluoro-2,3,3a,4,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)acetamide

To a solution of 9-fluoro-1,2,3,3a,4,5,5a,6-octahydropyrrolo[1,2-a]quinoxaline (5.6 g, 29.1 mmol), diisopropylethyl amine (30.5 mL, 175 mmol) in dimethylformamide (DMF) (100 ml), 2-bromoacetamide (16.08 g, 117 mmol) was added and the reaction solution was stirred 12 h at 100° C. After cooling to 20° C., water (300 ml) was added, and the mixture was extracted with ethyl acetate (3×200 ml); the organic layer was dried over anhydrous Na₂SO₄, concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (dichloromethane: methanol=100:1 to 50:1) to give the title compound (3 g, 12.03 mmol, yield 41.3%).

LCMS (ESI+): m/z 250 (M+H)⁺

57.6 Preparation of 2-(9-fluoro-2,3,3a,4,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)ethanamine

To a solution of 2-(9-fluoro-2,3,3a,4,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)acetamide (3 g, 12.03 mmol) in THF (20 ml), a solution of BH₃.THF (3.1 g, 36.1 mmol) was added at 0° C., then the reaction solution was stirred for 12 h at 70° C. After cooling to 0° C., methanol (100 ml) was added at 0° C., and the reaction solution was stirred for 30 minutes at 20° C. Then the solution was concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (petrol ether/ethyl acetate=20:1 to 10:1) to give title compound (1.3 g, 5.52 mmol, yield 45.9%).

¹H NMR (400 MHz, CD₃OD): δ[ppm]: 6.63-6.59 (m, 1H), 6.48 (d, J=8.4 Hz, 1H), 6.34-6.29 (m, 1H), 3.73-3.70 (m, 1H), 3.34-3.25 (m, 3H), 3.11-3.08 (m, 1H), 2.84-2.79 (m, 3H), 2.64-2.61 (m, 1H), 2.13-2.09 (m, 1H), 1.80-1.76 (m, 2H), 1.55-1.51 (m, 1H)

57.7 Preparation of 1-fluoro-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

To a solution of 2-(9-fluoro-2,3,3a,4,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)ethanamine (1.1 g, 4.67 mmol) and formaldehyde (2.106 g, 70.1 mmol) in ethanol (20 ml), trifluoroacetic acid (TFA) (2.88 mL, 37.4 mmol) was added, and the reaction solution was stirred for 12 h at 90° C. After cooling to 40° C., the solution was concentrated under reduced pressure, and the residue was purified by prep-HPLC to give the title compound as TFA salt (1.087 g, yield 94%).

Prep-HPLC Method:

Instrument: Shimadzu LC-20AP preparative HPLC

Column: Luna(2) C18 250*50 mm i.d. 10 u

Mobile phase: A for H₂O (0.09% TFA1) and B for CH₃CN

Gradient: B from 0% to 20% in 20 min

Flow rate: 80 ml/min

Wavelength: 220 &254 nm

Injection amount: 1.1 g per injection

¹H NMR (400 MHz, CD₃OD): δ[ppm]: 6.79-6.71 (m, 2H), 4.23 (s, 2H), 4.01-3.96 (m, 1H), 3.36-3.32 (m, 3H), 3.29-3.27 (m, 2H), 3.15-3.12 (m, 2H), 2.49-2.43 (m, 1H), 2.29-2.21 (m, 1H), 1.95-1.90 (m, 2H), 1.58-1.54 (m, 1H)

Example 58 1-Bromo-5,6,7,9,9a,10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (Compound of the Formula I.a in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-868 of Table A) 58.1 Preparation of 1-(2-bromo-6-nitro-phenyl)-pyrrolidine-2-carboxylate

A mixture of 1-bromo-2-fluoro-3-nitrobenzene (60 g, 273 mmol), methyl pyrrolidine-2-carboxylate (54.2 g, 327 mmol; see example 57.1) and triethylamine (83 g, 818 mmol) was heated at 70° C. for 16 h. Then the mixture was cooled, diluted with ethyl acetate (1000 ml), washed with 2N HCl (500 ml), aqueous K₂CO₃ (300 ml) and brine (300 ml) sequentially, and the aqueous phase was extracted with ethyl acetate (500 ml) again. The ethyl acetate layer was dried over Na₂SO₄, filtered, concentrated, and the residue was purified by column chromatography on silica gel (eluted with petrol ether/ethyl acetate=50:1 to 10:1) to afford the title compound (66 g, yield 74%) as yellow solid.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.80-7.78 (m, 1H), 7.64-7.62 (m, 1H), 7.19 (t, J=8.2 Hz, 1H), 4.26-4.16 (m, 1H), 3.70-3.65 (m, 1H), 3.59 (s, 3H), 3.36-3.23 (m, 1H), 2.40-2.23 (m, 2H), 2.15-2.04 (m, 2H)

58.2 Preparation of 9-bromo-2,3,3a,5,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-4-one

To a solution of 1-(2-bromo-6-nitro-phenyl)-pyrrolidine-2-carboxylate (45 g, 137 mmol) in methanol (225 ml) was added a solution of NH₄Cl (65.8 g, 1230 mmol) in water (225 ml) and Fe powder (53.4 g, 957 mmol) at 23° C., and the resulting mixture was heated at 85° C. for 1.5 h. Then the reaction was cooled, diluted with methanol (1000 ml), and the resulting mixture was stirred for 10 minutes, filtered, and the filter cake was washed with methanol (500 ml). The filtrate was concentrated under reduced pressure, the residue was put into water, extracted with ethyl acetate (3×800 ml), the extracts were washed with brine (400 ml), dried over Na₂SO₄, filtered, and concentrated to afford the title compound (33 g, yield 90%) as a light yellow solid.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 9.78 (s, 1H), 7.27-7.17 (m, 1H), 6.91-6.75 (m, 2H), 4.10-3.90 (m, 2H), 3.09-3.06 (m, 1H), 2.86-2.68 (m, 1H), 2.37-2.20 (m, 1H), 2.04-2.02 (m, 1H), 1.88-1.68 (m, 1H)

58.3 Preparation of 9-bromo-1,2,3,3a,4,5,5a,6-octahydropyrrolo[1,2-a]quinoxaline

To a solution of 9-bromo-2,3,3a,5,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-4-one (24 g, 90 mmol) in THF (360 ml) was added dropwise BH₃.DMS (50 ml, 500 mmol, 10 M in dimethylsulfide (DMS)) at 23° C., and the resulting solution was stirred at 70° C. for 2 h. The reaction was then cooled, and quenched with methanol. One additional reaction was set up and quenched as described above. The two resulting mixtures were combined, concentrated to about one third of volume, 6N HCl (250 mL) was added, and the resulting solution was heated at 70° C. for 20 minutes. Then the solution was cooled, adjusted to pH 9 by addition of saturated aqueous K₂CO₃, extracted with ethyl acetate (3×400 mL), the extracts were washed with brine, dried over Na₂SO₄, concentrated to give the residue, which was purified by column chromatography on silica gel (eluted with petrol ether/ethyl acetate=20:1 to 5:1) to afford the title compound (40 g, yield 88%) as a white solid.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 6.93-6.91 (m, 1H), 6.66 (t, J=7.7 Hz, 1H), 6.54-6.51 (m, 1H), 4.24-4.20 (m, 1H), 4.08 (s, 1H), 3.37-3.35 (m, 1H), 3.14-.311 (m, 1H), 2.89-2.76 (m, 1H), 2.76-2.62 (m, 1H), 2.37-2.22 (m, 1H), 1.96-1.93 (m, 1H), 1.89-1.77 (m, 1H), 1.75-1.63 (m, 1H).

58.4 Preparation of 2-(9-bromo-2,3,3a,4,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)acetamide

A mixture of 9-bromo-1,2,3,3a,4,5,5a,6-octahydropyrrolo[1,2-a]quinoxaline (20 g, 79 mmol), 2-bromoacetamide (32.7 g, 237 mmol), and DIEA (51.1 g, 395 mmol) in DMF (200 mL) was stirred at 100° C. for 15 h. The reaction was cooled, diluted with water (600 ml), and extracted with ethyl acetate (3×400 ml). The organic layers were washed with brine (200 ml), dried over Na₂SO₄ and filtered, concentrated to give a residue, which was recrystallized from ethyl acetate to afford the title compound (22 g, yield 90%) as a light yellow solid.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.04 (d, J=7.9 Hz, 1H), 6.75 (t, J=7.9 Hz, 1H), 6.55 (d, J=7.9 Hz, 1H), 6.39 (s, 1H), 5.69 (s, 1H), 4.28-4.25 (m, 1H), 3.96-3.75 (m, 2H), 3.55-3.42 (m, 1H), 3.13-3.04 (m, 1H), 3.03-2.91 (m, 1H), 2.77-2.65 (m, 1H), 2.39-2.23 (m, 1H), 2.04-1.90 (m, 1H), 1.90-1.78 (m, 1H), 1.71-1.67 (m, 1H)

58.5 Preparation of 2-(9-bromo-2,3,3a,4,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)ethanamine

To a solution of 2-(9-bromo-2,3,3a,4,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)acetamide (11 g, 35.5 mmol) in THF (165 ml) was added dropwise BH₃.DMS (18 ml, 180 mmol, 10 M in DMS) at 23° C., and the resulting solution was heated at 70° C. for 4 h. The reaction was then quenched with methanol. One additional reaction was set up and quenched as described above. The two resulting mixtures were combined, concentrated to about one third of volume, 6N HCl (200 mL) was added, and the resulting solution was heated at 70° C. for 20 minutes. The solution was then cooled, adjusted to pH 9 by addition of saturated aqueous K₂CO₃, and extracted with ethyl acetate (3×300 m). The extracts were washed with brine, dried over Na₂SO₄ and concentrated to give a residue, which was purified by column chromatography on silica gel (eluted with dichloromethane/methanol=60:1 to 15:1) to afford the title compound (15 g, yield 71%) as a light yellow oil.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 6.94-6.87 (m, 1H), 6.78-6.67 (m, 2H), 4.25-4.21 (m, 1H), 3.51-3.40 (m, 1H), 3.39-3.28 (m, 2H), 3.07-3.05 (m, 1H), 3.02-2.84 (m, 3H), 2.67-2.57 (m, 1H), 2.29-2.27 (m, 1H), 2.00-1.87 (m, 1H), 1.87-1.74 (m, 1H), 1.71-1.60 (m, 1H), 1.26 (s, 2H)

58.6 Preparation of 1-bromo-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

To a solution of 2-(9-bromo-2,3,3a,4,5a,6-hexahydro-1H-pyrrolo[1,2-a]quinoxalin-5-yl)ethanamine (13 g, 43.9 mmol) in ethanol (390 ml) was added formaldehyde (7.1 g, 88 mmol, 37% aqueous) and TFA (15 g, 132 mmol), and the resulting solution was heated at 80° C. for 2 h. Then the reaction was concentrated, the residue was dissolved in ethyl acetate (300 ml), and washed with saturated aqueous K₂CO₃ (150 ml), and brine (100 ml). The ethyl acetate layer was dried over Na₂SO₄, filtered, and concentrated to afford the title compound (13 g, crude) as a yellow solid.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.17-7.08 (m, 1H), 6.69-6.60 (m, 1H), 4.40-4.27 (m, 1H), 3.96-3.78 (m, 2H), 3.24-3.14 (m, 1H), 3.13-3.02 (m, 2H), 3.01-2.88 (m, 3H), 2.79-2.70 (m, 1H), 2.66-2.58 (m, 1H), 2.36-2.28 (m, 1H), 2.23 (s, 1H), 1.99-1.88 (m, 1H), 1.83-1.71 (m, 1H), 1.71-1.61 (m, 1H)

Analytical Method: The gradient was 1-90% B in 3.4 min, 90-100% B in 0.45 min, 100-1% B in 0.01 min, and then held at 1% B for 0.65 min (0.8 mL/min flow rate). Mobile phase A was 0.0375% TFA in water, mobile phase B was 0.018% TFA in acetonitril.

The column used for the chromatography was a 2.1×50 mm Venusil XBP-C18 column (5 m particles). Detection methods are diode array (DAD) and evaporative light scattering (ELSD) detection as well as positive/negative electrospray ionization.).

Example 59 1-Methyl-5,6,7,9,9a,10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline, trifluoroacetic acid (Compound of the Formula I.a in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-869 of Table A) 59.1 Preparation of boc-protected 1-bromo-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

To a solution of 1-bromo-5,6,7,9,9a,10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (13 g, 42.2 mmol) in dichloromethane (DCM) (260 ml) were added triethylamine (6.4 g, 63.3 mmol) and a solution of Boc₂O (10.1 g, 46.4 mmol) in DCM (20 ml) at 0° C., then it was allowed to warm to 23° C. and stirred for 16 h. The reaction was diluted with DCM (250 ml), washed with 2 N HCl (200 ml), saturated aqueous K₂CO₃ (150 ml) and brine (150 ml), and the water phase was extracted with DCM (200 mL) again. The combined organic layers were dried over Na₂SO₄, filtered, and concentrated, and the residue was purified by column chromatography on silica gel (eluted with petrol ether/ethyl acetate=30:1 to 4:1) to give the boc-protected compound (6 g, yield 35%, 2 steps).

LCMS (ESI+): m/z 408 (M+H)⁺

¹H NMR (400 MHz; CD₃OD): δ[ppm]: 7.11 (d, J=7.50 Hz, 1H), 6.73 (d, J=7.94 Hz, 1H), 4.67-4.50 (m, 1H), 4.36-4.24 (m, 1H), 4.18-4.01 (m, 1H), 3.91 (d, J=11.91 Hz, 1H), 3.27 (s, 1H), 3.20-2.90 (m, 4H), 2.76-2.55 (m, 2H), 2.27-2.25 (m, 1H), 1.97-1.66 (m, 3H), 1.46 (m, 9H)

59.2 Preparation of boc-protected 1-methyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

To a mixture of boc-protected 1-bromo-5,6,7,9,9a,10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (500 mg, 1.2 mmol), tricyclohexylphosphine (34.3 mg, 0.12 mmol), and Pd(OAc)₂ (13.7 mg, 0.06 mmol) in toluene (20 ml) under N₂ atmosphere was added methylboronic acid (366 mg, 6.1 mmol), K₃PO₄ (1.04 g, 4.9 mmol) and Water (2 mL). The reaction mixture was heated at 100° C. for 16 h. After cooling, the reaction mixture was diluted with ethyl acetate (100 ml) and washed with brine. The organic layer was dried over Na₂SO₄, filtered and concentrated. The residue was purified by column chromatography on silica gel (eluted with petrol ether/ethyl acetate=25:1 to 4:1) to afford the title compound (0.35 g, yield 73%) as white solid.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 6.95-6.49 (m, 2H), 4.81-4.48 (m, 1H), 4.20-3.68 (m, 3H), 3.52-3.17 (m, 2H), 3.11-2.81 (m, 3H), 2.78-2.51 (m, 2H), 2.32 (s, 3H), 2.01-1.86 (m, 1H), 1.86-1.71 (m, 1H), 1.71-1.60 (m, 1H), 1.44 (s, 9H)

59.3 Preparation of 1-methyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

To a solution of boc-protected 1-methyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (350 mg, 0.9 mmol) in DCM (6 ml) was added TFA (3 ml), and the resulting solution was stirred at 20° C. for 5 h. The reaction was then concentrated and the residue was purified by Prep-HPLC and lyophilized to afford the title compound (242 mg, yield 92%, TFA salt) as a light gray solid.

¹H NMR (400 MHz; CD₃OD): δ[ppm]: 7.12 (d, J=7.5 Hz, 1H), 6.97-6.86 (m, 1H), 4.34-4.22 (m, 2H), 4.16-4.11 (m, 1H), 3.69-3.66 (m, 1H), 3.54-3.43 (m, 1H), 3.39-3.33 (m, 2H), 3.30-3.23 (m, 2H), 3.10-2.97 (m, 2H), 2.43 (s, 3H), 2.41-2.31 (m, 1H), 2.13-1.98 (m, 2H), 1.95-1.85 (m, 1H)

Example 60 1-Cyclopropyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline, trifluoroacetic acid (Compound of the Formula I.a in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-873 of Table A)

The compound was prepared in analogy to example 59.

LCMS (ESI+): m/z 270 (M+H)⁺

¹H NMR (400 MHz; CD₃OD): δ[ppm]: 7.10 (d, J=7.9 Hz, 1H), 6.67 (d, J=7.9 Hz, 1H), 4.41-4.38 (m, 1H), 4.26 (s, 2H), 3.67-3.66 (m, 1H), 3.52-3.42 (m, 1H), 3.39-3.33 (m, 2H), 3.29-3.21 (m, 2H), 3.15-3.09 (m, 1H), 3.00-2.87 (m, 1H), 2.46-2.31 (m, 1H), 2.17-1.94 (m, 3H), 1.93-1.82 (m, 1H), 1.20-1.17 (m, 1H), 1.07-0.93 (m, 2H), 0.69-0.54 (m, 1H).

Example 61 1-Cyclobutyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (Compound of the Formula I.a in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-874 of Table A) 61.1 Preparation of boc-protected 1-(1-hydroxy-cyclobut-1-yl)-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

To a solution of boc-protected 1-bromo-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (800 mg, 1.96 mmol) in THF (16 ml) was added dropwise n-BuLi (1.6 ml, 3.92 mmol, 2.5 M in hexane) at −70° C. with stirring under N₂ atmosphere, and the resulting solution was stirred at −70° C. for 1 hour. A solution of cyclobutanone (275 mg, 3.92 mmol) in THF (0.5 ml) was added dropwise at −70° C., and the reaction solution was stirred for 2 h at same temperature. Then it was allowed to warm slowly to 20° C. and stirred for 16 h. The reactiont was quenched by saturated aqueous NH₄Cl, extracted with ethyl acetate (2×100 ml), the organic layers were dried over Na₂SO₄, concentrated, and the residue was purified by column chromatography on silica gel (eluted with petrol ether/ethyl acetate=10:1 to 2:1) to afford the title compound (0.5 g, yield 64%) as white solid.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.07-6.90 (m, 2H), 4.64-4.48 (m, 1H), 4.23 (d, J=14.1 Hz, 1H), 3.86 (d, J=11.5 Hz, 1H), 3.68-3.67 (m, 1H), 3.52-3.31 (m, 1H), 3.25-3.11 (m, 2H), 3.10-2.94 (m, 2H), 2.94-2.76 (m, 2H), 2.60-2.47 (m, 2H), 2.46-2.33 (m, 2H), 2.29-2.16 (m, 1H), 2.01-1.82 (m, 3H), 1.82-1.68 (m, 1H), 1.68-1.54 (m, 1H), 1.41 (s, 9H).

61.2 Preparation of 1-cyclobutyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

To a solution of boc-protected 1-(1-hydroxy-cyclobut-1-yl)-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (380 mg, 0.95 mmol) in DCM (3 ml) was added triethylsilane (1.66 g, 14.3 mmol), and the resulting solution was stirred for 0.5 h. Then TFA (10 ml) was added, and the resulting solution was stirred at 60° C. overnight. The solvent was removed under reduced pressure. The residue was dissoved in 3 N HCl (50 ml), and washed with DCM (3×50 ml). The aqueous phase was adjusted to pH 9 by addition of saturated aqueous K₂CO₃, the resulting mixture was extracted with DCM (2×100 ml), the DCM layers were washed with brine (30 ml), dried over Na₂SO₄, filtered, and concentrated to afford the title compound (160 mg, yield 60%) as a gray solid.

LCMS (ESI+): m/z 284 (M+H)⁺

¹H NMR (400 MHz; CD₃OD): δ[ppm]: 6.91 (d, J=7.9 Hz, 1H), 6.79 (d, J=7.5 Hz, 1H), 3.89-3.71 (m, 3H), 3.69-3.60 (m, 1H), 3.17-3.05 (m, 1H), 3.05-2.84 (m, 5H), 2.68-2.48 (m, 2H), 2.48-2.36 (m, 1H), 2.33-2.18 (m, 2H), 2.17-1.93 (m, 3H), 1.93-1.74 (m, 3H), 1.68-1.54 (m, 1H)

Example 62 1-Cyclopentyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline, trifluoroacetic acid (Compound of the Formula I.a in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-875 of Table A) 62.1 Preparation of boc-protected 1-(1-hydroxy-cyclopent-1-yl)-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

To a solution of boc-protected 1-bromo-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (100 mg, 0.25 mmol) in THF (2 ml) was added dropwise n-BuLi (0.2 ml, 0.5 mmol, 2.5 M in hexane) at −70° C. with stirring under N₂ atmosphere, and the resulting solution was stirred at −70° C. for 1 hour. A solution of cyclopentanone (40 mg, 0.5 mmol) in THF (0.2 ml) was added dropwise at −70° C., and the reaction solution was stirred for 8 h at same temperature. It was then allowed to warm slowly to 20° C. and stirred for 16 h. The reaction was quenched by saturated aqueous NH₄Cl, extracted with ethyl acetate (2×50 ml), the organic layers were dried over Na₂SO₄, concentrated, and the residue was purified by Prep-TLC (petrol ether/ethyl acetate=2:1) to afford the title compound (16 mg, yield 22%) as white solid.

¹H NMR (400 MHz; DMSO-d₆ (T=273+80 K)): δ[ppm]: 7.50 (s, 1H), 6.81-6.75 (m, 1H), 6.74-6.68 (m, 1H), 4.46-4.24 (m, 2H), 3.75-3.66 (m, 2H), 3.42-3.26 (m, 2H), 3.24-3.12 (m, 2H), 2.93 (d, J=9.7 Hz, 1H), 2.63-2.51 (m, 2H), 2.15-2.03 (m, 4H), 1.99-1.90 (m, 1H), 1.83-1.82 (m, 5H), 1.72-1.55 (m, 3H), 1.34 (s, 9H)

62.2 Preparation of boc-protected 1-cyclopent-1-enyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

A mixture of boc-protected 1-(1-hydroxy-cyclopent-1-yl)-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (100 mg, 0.25 mmol), 2-(cyclopent-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (95 mg, 0.49 mmol), Pd(PPh₃)₂Cl₂ (12 mg, 0.017 mmol) and Cs₂CO₃ (160 mg, 0.49 mmol) in dioxane (2 ml) and water (0.6 ml) was placed in a microwave tube under N₂ atmosphere. The reaction mixture was heated at 100 C for 1 hour in microwave reactor. Six additional reactions were set up as described above. All seven reaction mixtures were combined, was put into water, extracted with ethyl acetate (2×100 ml); the extracts were washed with brine, dried over Na₂SO₄, andconcentrated to give crude product, which was purified by column chromatography on silica gel (eleted with petrol ether/ethyl acetate=25:1 to 5:1) to afford the title compound (400 mg, yield 58%) as light yellow solid.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 6.93-6.68 (m, 2H), 5.94-5.78 (m, 1H), 4.81-4.52 (m, 1H), 4.15 (d, J=13.7 Hz, 1H), 4.08-3.78 (m, 1H), 3.71-3.58 (m, 1H), 3.45-3.17 (m, 2H), 3.15-2.85 (m, 4H), 2.69-2.41 (m, 4H), 2.38-2.18 (m, 2H), 2.02-1.96 (m, 2H), 1.86-1.66 (m, 2H), 1.59-1.51 (m, 1H), 1.44 (s, 9H)

62.3 Preparation of boc-protected 1-cyclopentyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

A mixture of 1-cyclopent-1-enyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (0.3 g, 0.76 mmol), and Pd/C (0.09 g, 5%) in methanol (20 ml) was stirred at 20° C. under a H₂ balloon for 16 h. Then the reaction was filtered, and concentrated to afford the title compound (0.29 g, yield 96%) as light yellow solid.

LCMS (ESI+): m/z 398 (M+H)⁺

62.4 Preparation of 1-cyclopentyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline

To a solution of boc-protected 1-cyclopentyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline (0.29 g, 0.74 mmol) in DCM (6 ml) was added TFA (3 ml), and the resulting solution was stirred for 3 h at 25° C. The reaction was concentrated and lyophilized to afford the title compound (351 mg, yield 90%, TFA salt) as brown oil.

¹H NMR (400 MHz; CD₃OD): δ[ppm]: 7.34 (d, J=8.4 Hz, 1H), 7.13 (d, J=7.9 Hz, 1H), 4.37-4.25 (m, 2H), 4.24-4.14 (m, 1H), 3.96-3.87 (m, 1H), 3.62-3.52 (m, 1H), 3.44-3.32 (m, 4H), 3.30-3.19 (m, 3H), 2.48-2.35 (m, 1H), 2.25-2.04 (m, 4H), 2.04-1.85 (m, 3H), 1.85-1.70 (m, 2H), 1.70-1.56 (m, 2H)

Example 63 8-Methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-8-ol (Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-241 of Table B) 63.1 Preparation of boc-protected ethyl 3-(2,3,4,5-tetrahydro-1,4-benzodiazepin-1-yl)propanoate

To a solution of 4-boc-protected 2,3,4,5-tetrahydro-1H-1,4-benzodiazepine (7 g, 28.2 mmol) in acetic acid (14 ml) was added ethyl acrylate (14.1 g, 141 mmol) and the reaction mixture was heated at 100° C. for 16 hrs. Then it was cooled, concentrated, and the residue was purified by column chromatography on silica gel (eluted with petrol ether/ethyl acetate=25:1 to 5:1) to give the title compound (5 g, yield 51%) as light yellow oil.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.32-7.14 (m, 2H), 7.03-6.88 (m, 2H), 4.43-4.26 (m, 2H), 4.20-4.08 (m, 2H), 3.64-3.51 (m, 4H), 3.10-2.99 (m, 2H), 2.63-2.53 (m, 2H), 1.49-1.38 (m, 9H), 1.30-1.19 (m, 3H)

63.2 Preparation of boc-protected 3-(2,3,4,5-tetrahydro-1,4-benzodiazepin-1-yl)propanoic acid

To a solution of boc-protected ethyl 3-(2,3,4,5-tetrahydro-1,4-benzodiazepin-1-yl)propanoate (7.5 g, 21.5 mmol) in THF (70 mL), H₂O (50 mL) and methanol (23 ml) was added a solution of NaOH (2.6 g, 64.6 mmol) in H₂O (20 mL) at 5° C., and the resulting solution was stirred at 25° C. for 3 h. Then the solution was cooled to 5° C., adjusted to pH 3 by addition of 1N HCl, and the resulting mixture was extracted with ethyl acetate three times. The ethyl acetate layers were combined, dried over Na₂SO₄, filtered, and concentrated to give the title compound (6.7 g, yield 97%) as yellow oil.

¹H NMR (400 MHz; CD₃OD): δ[ppm]: δ 7.23-7.06 (m, 2H), 6.98-6.85 (m, 2H), 4.39-4.21 (m, 2H), 3.65-3.41 (m, 4H), 3.05-2.91 (m, 2H), 2.56 (t, J=6.6 Hz, 2H), 1.40-1.31 (m, 9H).

63.3 Preparation of boc-protected 3-(2,3,4,5-tetrahydro-1,4-benzodiazepin-1-yl)propanoyl chloride

To a solution of boc-protected 3-(2,3,4,5-tetrahydro-1,4-benzodiazepin-1-yl)propanoic acid (6.5 g, 20.3 mmol) in dichloromethane (300 ml) were added dimethylformamide (0.15 g, 2 mmol) and dropwise a solution of (COCl)₂ (7.7 g, 60.9 mmol) in dichloromethane (30 ml) at 0° C. The the reaction was stirred for 1 hour at 25° C., and concentrated under reduced pressure below 30° C. to give the title compound as a residue which was used directly in the next step without further purification.

63.4 Preparation of boc-protected 1,2,3,4,6,7-hexahydro[1,4]diazepino[6,7,1-ij]-quinolin-8-one

To a solution of boc-protected 3-(2,3,4,5-tetrahydro-1,4-benzodiazepin-1-yl)propanoyl chloride (6.6 g, crude, −20 mmol) in dichloroethane (400 ml) was added A1Cl₃ (10.4 g, 78 mmol) in portions at 0-5° C., then the resulting mixture was stirred at 65° C. for 7 hrs.

The reaction was quenched with water (100 ml), adjusted to pH 9 by addition of aqueous saturated K₂CO₃, then Boc₂O (6.4 g, 29.2 mmol) was added, and the resulting mixture was stirred for 2 hrs. The mixture was extracted with dichloromethane twice, the organic phase was washed with brine, dried over Na₂SO₄, concentrated, and the residue was purified by column chromatography on silica gel (eluted with petrol ether/ethyl acetate=10:1 to 2:1) to give the title compound (4.2 g, yield 71%) as yellow solid.

¹H NMR (400 MHz, CDCl₃): δ[ppm]: 7.85 (d, J=7.5 Hz, 1H), 7.40-7.20 (m, 1H), 6.83 (t, J=7.5 Hz, 1H), 4.58-4.40 (m, 2H), 3.74 (d, J=3.5 Hz, 2H), 3.60-3.50 (m, 2H), 3.44-3.37 (m, 2H), 2.72-2.62 (m, 2H), 1.47-1.29 (m, 9H).

63.5 Preparation of 1,2,3,4,6,7-hexahydro[1,4]diazepino[6,7,1-ij]-quinolin-8-one

To a solution of boc-protected 1,2,3,4,6,7-hexahydro[1,4]diazepino[6,7,1-ij]-quinolin-8-one (500 mg, 1.7 mmol) in dichloromethane (10 ml) was added trifluoroacetic acid (5 ml), and then the resulting mixture was stirred at 25° C. for 3 hrs. This was concentrated and lyophilized to give the title compound (500 mg, yield 100%, trifluoroacetic acid salt) as yellow solid.

¹H NMR (400 MHz; CD₃OD): δ[ppm]: 7.92-790 (m, 1H), 7.49 (d, J=6.6 Hz, 1H), 6.97 (t, J=7.7 Hz, 1H), 4.40 (s, 2H), 3.71-3.63 (m, 4H), 3.55-3.47 (m, 2H), 2.75-2.67 (m, 2H).

63.6 Preparation of Cbz-protected 1,2,3,4,6,7-hexahydro[1,4]diazepino[6,7,1-ij]-quinolin-8-one

To a solution of 1,2,3,4,6,7-hexahydro[1,4]diazepino[6,7,1-ij]-quinolin-8-one (2 g, 6.92 mmol) (TFA salt) in DCM (30 ml) were added triethylamine (1.4 g, 13.8 mmol) and a solution of CbzCl (Cbz=benzyloxycarbonyl; 1.5 g, 9 mmol) in DCM (5 mL) at 0-5° C., then the reaction mixture was stirred at 25° C. for 2 hrs. Then it was diluted with DCM (100 ml), washed with aqueous K₂CO₃ (50 mL) and brine (50 ml); the water phase was extracted with DCM again, the DCM layer was dried over Na₂SO₄, filtered, and concentrated under reduced pressure to give the title compound (1.5 g, yield 64%) as brown oil.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.79 (d, J=7.6 Hz, 1H), 7.30-7.11 (m, 6H), 6.76-6.72 (m, 1H), 5.04-5.01 (m, 2H), 4.55-4.48 (m, 2H), 3.75-3.74 (m, 2H), 3.48-3.38 (m, 4H), 2.60-2.55 (m, 2H)

63.7 Preparation of Cbz-protected 8-methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-8-ol

To a solution of Cbz-protected 1,2,3,4,6,7-hexahydro[1,4]diazepino[6,7,1-ij]-quinolin-8-one (1.5 g, 4.5 mmol) in THF (45 ml) was added dropwise methyllithium (3.7 ml, 5.8 mmol, 1.6 M in ether) at −70° C., and the resulting solution was stirred at −70° C. for 2 h. Then it was quenched with aqueous NH₄Cl (20 ml), extracted with ethyl acetate (50 ml) three times, the ethyl acetate layers were washed with brine (30 ml), dried over Na₂SO₄, filtered, concentrated, and the residue was purified by column chromatography on silica gel (eluted with DCM/methanol=150:1 to 50:1) to give the title compound (1 g, yield 64%) as light yellow oil.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.47 (d, J=7.5 Hz, 1H), 7.39-7.25 (m, 5H), 7.25-6.99 (m, 1H), 6.93-6.80 (m, 1H), 5.18-5.02 (m, 2H), 4.62-4.35 (m, 2H), 3.79 s, 1H), 3.73-3.59 (m, 1H), 3.45-3.34 (m, 1H), 3.29-3.15 (m, 3H), 2.00-1.89 (m, 2H), 1.59 (s, 3H)

63.8 Preparation of 8-methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-8-ol

A mixture of Cbz-protected 8-hydroxy-8-methyl-1,2,3,4,7,8-hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline (0.5 g, 1.42 mmol), NH₃—H₂O (1 ml) and Pd/C (168 mg, 10%) in THF (30 ml) was stirred under a H₂ balloon for 2 h. Then it was filtered, concentrated, and the residue was purified by Prep-HPC (basic method) and lyophilized to give the title compound (214 mg, yield 69%) as white solid.

LCMS (ESI+): m/z 219 (M+H)⁺

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.44 (d, J=7.5 Hz, 1H), 7.01 (d, J=7.1 Hz, 1H), 6.83 (t, J=7.5 Hz, 1H), 3.92-3.81 (m, 2H), 3.43-3.32 (m, 1H), 3.29-3.17 (m, 1H), 3.14-3.00 (m, 4H), 1.99-1.91 (m, 2H), 1.59 (s, 3H)

Example 64 8-Methoxy-8-methyl-2,3,4,6,7,8-hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline (Compound of the Formula I.g, I.h or I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-201 of Table B) 64.1 Preparation of Cbz-protected 8-methoxy-8-methyl-1,2,3,4,7,8-hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline

To a solution of Cbz-protected 8-methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-8-ol (0.5 mg, 1.42 mmol; see example 63.2) in DMF (10 ml) was added NaH (113 mg, 2.84 mmol) in portions at 0-5° C., and then the resulting mixture was stirred at 25° C. for 0.5 hrs. A solution of MeI (403 mg, 2.84 mmol) in DMF (2 ml) was added dropwise at 0-5° C., then the reaction mixture was stirred at 25° C. for 16 h. It was quenched with water (30 ml), and extracted with ethyl acetate (60 ml) twice. The ethyl acetate layer was washed with brine, dried over Na₂SO₄, and concentrated to give a residue, which was purified by column chromatography on silica gel (eluted with petrol ether/ethyl acetate=15:1 to 4:1) to give the title compound (200 mg, yield 39%) as light yellow oil.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.41-7.24 (m, 6H), 7.23-7.01 (m, 1H), 6.93-6.79 (m, 1H), 5.12 (s, 2H), 4.64-4.49 (m, 1H), 4.44-4.34 (m, 1H), 3.88-3.75 (m, 1H), 3.69-3.58 (m, 1H), 3.40-3.26 (m, 2H), 3.23-3.12 (m, 2H), 3.08 (s, 3H), 2.28-2.19 (m, 1H), 1.72-1.63 (m, 1H), 1.53 (s, 3H)

64.2 Preparation of 8-methoxy-8-methyl-1,2,3,4,7,8-hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline

A mixture of Cbz-protected 8-methoxy-8-methyl-1,2,3,4,7,8-hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline (160 mg, 0.44 mmol), NH₃—H₂O (0.5 ml) and Pd/C (50 mg, 10%) in THF (20 ml) was stirred under a H₂ balloon at 25° C. for 2 hrs. Then it was filtered, concentrated, and the residue was purified by Prep-HPC (basic method) and lyophilized to give the title compound (55 mg, yield 54%) as yellow oil.

LCMS (ESI+): m/z 233 (M+H)⁺

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.30-7.27 (m, 1H), 7.02 (d, J=7.1 Hz, 1H), 6.83 (t, J=7.5 Hz, 1H), 3.94-3.84 (m, 2H), 3.38-3.24 (m, 2H), 3.16-3.01 (m, 7H), 2.27-2.22 (m, 1H), 1.69-1.63 (m, 1H), 1.54 (s, 3H)

Example 65 2,8-Dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-8-ol

A mixture of Cbz-protected 8-methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-8-ol (50 mg, 0.14 mmol; see example 63.2), formaldehyde (21 mg, 0.28 mmol, 40% in water) and Pd/C (17 mg, 10%) in methanol (5 ml) was stirred under a H₂ balloon for 6 hrs. Then it was filtered, concentrated, and the residue was purified by Prep-HPC (basic method) and lyophilized to give the title compound (12 mg, yield 36%) as light yellow solid.

¹H NMR (400 MHz; CDCl₃): δ[ppm]: 7.44-7.42 (m, 1H), 7.07-7.00 (m, 1H), 6.83 (t, J=7.5 Hz, 1H), 3.71-3.57 (m, 2H), 3.40-3.31 (m, 1H), 3.25-3.17 (m, 1H), 3.17-3.04 (m, 2H), 2.82 (t, J=5.1 Hz, 2H), 2.37 (s, 3H), 1.94 (t, J=6.0 Hz, 2H), 1.58 (s, 3H)

Example 66 11-Methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane], 2,2,2-trifluoroacetic acid (Compound of the Formula I.i in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-325 of Table B)

The title compound was prepared in analogy to example 1, using however tert-butyl 6-methyl-2,3,4,5-tetrahydro-1H-1,4-benzodiazepine-4-carboxylate and 2-cyclobutylidene-acetic acid as starting materials.

ESI-MS [M+H⁺]=243.20

¹H NMR (DMSO-d₆, 500 MHz) [ppm]: 7.28 (d, J=7.9 Hz, 1H), 6.71 (d, J=7.9 Hz, 1H), 3.74 (s, 2H), 3.10-3.03 (m, 2H), 2.99-2.94 (m, 2H), 2.90-2.84 (m, 2H), 2.34-2.25 (m, 2H), 2.22 (s, 3H), 2.09-1.96 (m, 1H), 1.92-1.83 (m, 5H).

Example 67 9-Methyl-1,2,3,4,6,7-Hexahydrospiro[[1,4]Diazepino[6,7,1-Ij]Quinoline-8,1′-Cyclobutane], Trifluoroacetic Acid (Compound of the Formula I.g in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-325 in Table B)

The intermediate tert-butyl 9-chloro-3,4,6,7-tetrahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]-2(1H)-carboxylate was prepared in analogy to example 1, steps 1.1 to 1.3 using tert-butyl 8-chloro-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate and 2-cyclobutylideneacetyl chloride as starting materials.

67.1 Preparation of tert-butyl 9-methyl-3,4,6,7-tetrahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]-2(1H)-carboxylate

75 mg (0.21 mmol) of tert-butyl 9-chloro-3,4,6,7-tetrahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]-2(1H)-carboxylate were dissolved in 0.5 ml of tetrahydrofurane, 0.5 ml toluene and 5 μl water. To this solution 35 μl (0.25 mmol) trimethylboroxine, 0.2 mg (0.4 μmol) of dicyclohexyl(2′,4′,6′-triisopropyl-[1,1′-biphenyl]-2yl)phosphine and 65.8 mg (0.31 mmol) of potassium phosphate were added and the solution was degassed with Argon. 0.1 mg (0.4 μmol) of palladium(II)acetate were added and the reaction mixture was heated at 100° C. for 10 minutes in a microwave unit. The reaction mixture was concentrated in vacuo. The residue was purified by column chromatography on silica (eluent: 0-30% methanol in dichloromethane) to yield 40 mg of the title compound.

ESI-MS [M+H⁺]=343.20

67.2 Preparation of 9-methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]-quinoline-8,1′-cyclobutane], trifluoroacetic acid

To 40 mg (0.12 mmol) of tert-butyl 9-methyl-3,4,6,7-tetrahydrospiro[[1,4]diazepino-[6,7,1-ij]quinoline-8,1′-cyclobutane]-2(1H)-carboxylate in 3 ml dichloromethane were added 90 μl (1.2 mmol) of trifluoroacetic acid at 0° C. The solution was stirred for 2 h at room temperature. The reaction mixture was concentrated in vacuo. The residue was purified by preparative HPLC to yield 4.6 mg of the title compound.

ESI-MS [M+H⁺]=243.20

¹H NMR (CDCl₃, 500 MHz): δ[ppm]: 9.15 (bs, 2H), 6.95 (d, 1H), 6.80 (d, 1H), 4.15 (m, 2H), 3.30 (m, 2H), 3.25 (m, 2H), 3.10 (m, 2H), 2.85 (m, 2H), 2.70 (s, 3H), 2.20 (m, 2H), 2.00 (m, 2H), 1.85 (m, 2H).

Example 68 4,5,6,7,9,9a,9b,10,10a, 11-Decahydrocyclopropa[3,4]pyrrolo[1,2-a][1,4]diazepino[1,7,6-de]quinoxaline

The title compound was prepared in analogy to example 44 using however 1-fluoro-2-nitrobenzene and ethyl 3-azabicyclo[3.1.0]hexane-2-carboxylate as starting materials.

ESI-MS [M+H⁺]=242.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.65 (m, 1H), 6.35 (d, 1H), 6.30 (d, 1H), 3.65 (m, 1H), 3.60 (m, 1H), 3.35 (m, 4H), 3.30 (m, 1H), 2.90 (m, 3H), 2.55 (m, 1H), 1.65 (m, 1H), 1.60 (m, 1H), 0.50 (m, 1H), 0.15 (m, 1H).

Example 69 1-Ethyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-289 in Table A)

The title compound was prepared in analogy to example 33, using however acetaldehyde instead of cyclobutanone.

ESI-MS [M+H⁺]=218.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.70 (m, 1H), 6.60 (d, 1H), 6.40 (d, 1H), 3.65 (s, 2H), 3.35 (m, 2H), 3.15 (m, 2H), 3.10 (m, 2H), 2.90 (m, 2H), 2.80 (m, 2H), 1.05 (t, 3H).

Example 70 1-Propyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.a, I.b or I.c in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-325 in Table A)

The title compound was prepared in analogy to example 33, using however propionaldehyde instead of cyclobutanone.

ESI-MS [M+H⁺]=232.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.70 (m, 1H), 6.60 (d, 1H), 6.40 (d, 1H), 3.65 (s, 2H), 3.25 (m, 2H), 3.15 (m, 4H), 2.90 (m, 2H), 2.80 (m, 2H), 1.50 (m, 2H), 0.90 (t, 3H).

Example 71 1-Cyclobutyl-5-methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.gg, I.hh or I.ii in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-433 in Table A)

The title compound was prepared in analogy to example 33, using tert-butyl 5-methyl-2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate and cyclobutanone. tert-Butyl 5-methyl-2,3,5,6-tetrahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline-7(8H)-carboxylate was prepared in analogy to example 30 however using 2-bromopropaneamide instead of 2-chloroacetamide and in analogy to example 32.

ESI-MS [M+H⁺]=258.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.65 (m, 1H), 6.55 (d, 1H), 6.45 (d, 1H), 3.90 (m, 1H), 3.80 (m, 1H), 3.55 (m, 1H), 3.30-3.15 (m, 3H), 3.10 (m, 1H), 2.95 (m, 1H), 2.85 (m, 1H), 2.75 (m, 1H), 2.20 (m, 1H), 2.15 (m, 1H), 2.05 (m, 2H), 1.65 (m, 2H), 0.9 (d, 3H).

Example 72 5-Methyl-1-(oxetan-3-yl)-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.gg, I.hh or I.ii in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-541 in Table A)

The title compound was prepared in analogy to example 71, using however oxetane-3-one instead of cyclobutanone.

ESI-MS [M+H⁺]=260.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.60 (m, 1H), 6.55 (d, 1H), 6.05 (d, 1H), 4.80 (m, 1H), 4.75 (m, 1H), 4.65 (m, 1H), 4.60 (m, 1H), 4.45 (m, 1H), 3.80 (d, 1H), 3.50 (d, 1H), 3.35 (m, 2H), 3.15 (m, 2H), 2.90 (m, 1H), 2.85 (m, 1H), 2.75 (m, 1H), 0.9 (d, 3H).

Example 73 1-Ethyl-5-methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.gg, I.hh or I.ii in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-289 in Table A)

The title compound was prepared in analogy to example 71, using however acetaldehyde instead of cyclobutanone.

ESI-MS [M+H⁺]=232.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.80 (m, 1H), 6.65 (d, 1H), 6.50 (d, 1H), 3.95 (d, 1H), 3.80 (d, 1H), 3.45-3.05 (m, 8H), 2.85 (m, 1H), 1.15 (t, 3H), 1.00 (d, 3H).

Example 74 5-Methyl-1-propyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline (Compound of the Formula I.gg, I.hh or I.ii in which the Combination of R^(5a), R^(5b), R⁶ and R^(9a) is as in Row A-325 in Table A)

The title compound was prepared in analogy to example 71, using however propionaldehyde instead of cyclobutanone.

ESI-MS [M+H⁺]=246.20

¹H NMR (DMSO-d₆, 500 MHz): δ[ppm]: 6.80 (m, 1H), 6.60 (d, 1H), 6.50 (d, 1H), 3.95 (d, 1H), 3.80 (d, 1H), 3.30 (m, 4H), 3.20 (m, 2H), 3.10 (m, 1H), 3.00 (m, 1H), 2.80 (m, 1H), 1.60 (m, 2H), 0.95 (d, 3H), 0.90 (t, 3H).

Example 75 9-Chloro-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-Cyclobutane], Trifluoroacetic Acid (Compound of the Formula I.g in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-323 in Table B)

The title compound was prepared in analogy to example 1 using tert-butyl 8-chloro-2,3-dihydro-1H-benzo[e][1,4]diazepine-4(5H)-carboxylate and 2-cyclobutylideneacetyl chloride as starting materials.

ESI-MS [M+H⁺]=236.10

¹H NMR (CDCl₃, 500 MHz): δ[ppm]: 9.60 (bs, 2H), 7.00 (m, 2H), 4.15 (s, 2H), 3.25 (m, 6H), 3.10 (m, 2H), 2.15 (m, 2H), 2.05 (m, 2H), 1.75 (m, 2H).

Example 76 10-Methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane], trifluoroacetic acid (Compound of the Formula I.h in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-325 in Table B) ESI-MS [M+H⁺]=243.20

¹H NMR (CDCl₃, 500 MHz): δ[ppm]: 9.35 (bs, 2H), 7.40 (s, 1H), 6.90 (s, 1H), 4.15 (m, 2H), 3.35 (m, 2H), 3.25 (m, 2H), 3.15 (m, 2H), 2.40 (m, 2H), 2.30 (s, 3H), 2.15-1.90 (m, 6H).

Example 77 10-Chloro-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane], trifluoroacetic acid (Compound of the Formula I.h in which the Combination of R^(5a), R^(5b), R⁷, R⁸ and R^(9a) is as in Row B-323 in Table B)

ESI-MS [M+H⁺]=236.10

¹H NMR (CDCl₃, 500 MHz): δ[ppm]: 9.65 (bs, 2H), 7.55 (s, 1H), 7.05 (s, 1H), 4.15 (s, 2H), 3.30 (m, 4H), 3.20 (m, 2H), 2.35 (m, 2H), 2.15-1.90 (m, 6H).

II. BIOLOGICAL TESTS Functional Activity

The functional activity of compounds of formula I was assayed by incubation with U2OS_HTR_(2C)_β-Arrestin cells (DiscoverX, 93-0289C3) to induce beta-arrestin2 recruitment to the 5-HT_(2C) receptor. The agonist-induced recruitment and proximity of the receptor and beta-arrestin2 leads to complementation and formation of active β-galactosidase. The enzyme complementation results in enzyme activity, which is measured following the termination of the agonist incubation using DiscoveRx's detection reagent, which contains a chemiluminescent substrate which produces a high intensity signal. Cells were plated and a medium-change to a 1% serum containing medium was performed 24 h later. The next day, test compounds were added and incubated for 1.5 h before addition of detection reagent.

The response produced was measured and compared with the response produced by 10 [mu]M 5-HT or the maximal effect induced by 5-HT (defined as 100%) to which it was expressed as a percentage response (relative efficacy). Dose response curves were constructed using Graphpad Prism (Graph Software Inc.) or using in house adapted software using a 4 parameter dose response model with variable slope (fit=(Bottom+(Top−Bottom)/(1+10{circumflex over ( )}((LogEC50−x)*HillSlope))res=(y−fit)). Results are compiled in the table below.

TABLE # Potency (EC50) in functional assay % efficacy 1 ++ 71 6 ++ 63 8 ++ 40 9 +++ 61 16 + 55 17 ++ 84 19 ++ 25 22 ++ 69 25 ++ 90 26 +++ 107 27 + 87 28 ++ 55 33 + 78 35 ++ 112 36 + 31 37 + 21 40 ++ 131 41 + 75 42 +++ 163 43 + 59 44 ++ 55 45 ++ 77 46 + 71 47 ++ 59 48 ++ 105 49 + 78 51 ++ 102 54 + 24 55 + 26 56 +++ 124 57 + 35 59 ++ 51 66 + 53 67 +++ 116 68 ++ 76 69 + 54 70 ++ 63 76 +++ 98 Potency (EC50): + from 200 nM to <1 μM ++ from 20 nM to <200 nM +++ <20 nM 

1. A compound of the formula (I)

wherein G is (CR^(3a)R^(3b))_(n); X is NR⁶ or CR⁷R⁸; R¹ is selected from the group consisting of hydrogen, cyano, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, —C(═O)R¹⁰, phenyl, phenyl-C₁-C₂-alkyl and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated heterocyclic ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups as ring members, where the cyclic moieties in the three last-mentioned radicals may be substituted with one or more substituents R¹¹; each R² is independently selected from the group consisting of cyano, nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the cyclic moieties in the six last-mentioned radicals may be substituted with one or more substituents R¹¹; R^(3a) and R^(3b), independently of each other, are selected from the group consisting of hydrogen, cyano, nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the cyclic moieties in the six last-mentioned radicals may be substituted with one or more substituents R¹¹; R^(4a) and R^(4b), independently of each other, are selected from the group consisting of hydrogen, cyano, nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), —NR^(12a)C(O)R¹, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the cyclic moieties in the six last-mentioned radicals may be substituted with one or more substituents R; or R^(4a) and R^(4b) form together a group ═O or ═S; R^(5a) and R^(5b), independently of each other, are selected from the group consisting of hydrogen, deuterium, halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the cyclic moieties in the six last-mentioned radicals may be substituted with one or more substituents R¹¹; where R^(5a) and R^(5b) are not simultaneously hydroxy; or R^(5a) and R^(5b), together with the carbon atom they are bound to, form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring, where the ring may contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and where the ring may be substituted with one or more substituents R; or R^(5a) and R⁶, together with the atoms they are bound to, form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated heterocyclic ring, where the ring may further contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and where the ring may be substituted with one or more substituents R¹¹; or R^(5a) and R⁷, together with the carbon atoms they are bound to, form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring, where the ring may contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and where the ring may be substituted with one or more substituents R¹¹; R⁶ is selected from the group consisting of hydrogen, cyano, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₃-C₈-cycloalkyl-C₁-C₄-alkyl, fluorinated C₃-C₈-cycloalkyl-C₁-C₄-alkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, —C(═O)R¹⁰, —SO₂R¹⁰, phenyl, phenyl-C₁-C₂-alkyl and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated heterocyclic ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO and SO₂ and optionally also 1 or 2 C═O and/or C═S groups as ring members, where the cyclic moieties in the three last-mentioned radicals may be substituted with one or more substituents R¹¹; R⁷ and R⁸, independently of each other, are selected from the group consisting of deuterium, halogen, cyano, nitro, hydroxyl, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the cyclic moieties in the six last-mentioned radicals may be substituted with one or more substituents R¹¹; where R⁷ and R⁸ are not simultaneously hydroxyl; and where R⁷ is not hydroxyl if R⁸ is C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, phenoxy or benzyloxy; or R⁷ and R⁸, together with the carbon atom they are bound to, form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring, where the ring may contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and where the ring may be substituted with one or more substituents R¹¹; each R⁹ is independently selected from the group consisting of halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₃-C₈-cycloalkenyl, fluorinated C₃-C₈-cycloalkenyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated C₁-C₆-alkylsulfonyl, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), —NR^(12a)C(O)R¹⁰, —C(═O)R¹⁰, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy, fluorinated C₁-C₆-alkylcarbonyloxy, phenyl, phenyl-C₁-C₂-alkyl, phenoxy, phenylsulfonyl, benzyloxy and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the cyclic moieties in the six last-mentioned radicals may be substituted with one or more substituents R¹¹; or two radicals R⁹ bound on neighboring carbon atoms, together with the carbon atoms they are bound to, form a 3-, 4-, 5-, 6-, 7- or 8-membered partially unsaturated or maximally unsaturated ring, where the ring may contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and where the ring may be substituted with one or more substituents R¹¹; each R¹⁰ is independently selected from the group consisting of hydrogen, cyano, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, —NR^(12a)R^(12b), CH₂NR^(12a)R^(12b), phenyl, phenyl-C₁-C₂-alkyl, phenoxy, benzyloxy and a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated ring containing 1, 2, 3 or 4 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members, where the cyclic moieties in the five last-mentioned radicals may be substituted with one or more substituents R¹¹; each R¹¹ is independently selected from the group consisting of halogen, cyano, nitro, hydroxy, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-hydroxyalkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkoxy-C₁-C₄-alkyl, C₁-C₆-hydroxyalkoxy, C₁-C₆-alkoxy-C₁-C₄-alkoxy, C₁-C₆-alkylthio, fluorinated C₁-C₆-alkylthio, C₁-C₆-alkylsulfinyl, fluorinated C₁-C₆-alkylsulfinyl, C₁-C₆-alkylsulfonyl, fluorinated C₁-C₆-alkylsulfonyl, —COOH, —NR^(12a)R^(12b), —CH₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyl, fluorinated C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, fluorinated C₁-C₆-alkoxycarbonyl, SO₂NR^(12a)R^(12b), C₁-C₆-alkylcarbonyloxy and fluorinated C₁-C₆-alkylcarbonyloxy; or two radicals R¹¹, together with the atom(s) they are bound to, form a saturated, partially unsaturated or maximally unsaturated 3-, 4-, 5-, 6- or 7-membered carbocyclic or heterocyclic ring, where the heterocyclic ring contains 1, 2 or 3 heteroatoms or heteroatom groups independently selected from N, O, S, NO, SO, SO₂, C═O and C═S as ring members; R^(12a) and R^(12b), independently of each other and independently of each occurrence, are selected from the group consisting of hydrogen, cyano, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₂-C₆-alkenyl, fluorinated C₂-C₆-alkenyl, C₂-C₆-alkynyl, fluorinated C₂-C₆-alkynyl, C₃-C₈-cycloalkyl, fluorinated C₃-C₈-cycloalkyl, C₁-C₆-alkoxy, fluorinated C₁-C₆-alkoxy, C₁-C₆-alkylcarbonyl, fluorinated C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, fluorinated C₁-C₆-alkoxycarbonyl, phenyl and benzyl, where the phenyl moieties in the two last-mentioned radicals may carry 1, 2 or 3 substituents selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy; or, if R^(12a) and R^(12b) are bound to the same nitrogen atom, together with this nitrogen atom may form a 3-, 4-, 5-, 6-, 7- or 8-membered saturated, partially unsaturated or maximally unsaturated heterocyclic ring, where the ring may further contain 1, 2, 3 or 4 heteroatoms or heteroatom-containing groups selected from O, S, N, SO, SO₂, C═O and C═S as ring members, and where the ring may be substituted with one or more substituents selected from halogen, cyano nitro, C₁-C₆-alkyl, fluorinated C₁-C₆-alkyl, C₁-C₆-alkoxy and fluorinated C₁-C₆-alkoxy; a is 0, 1 or 2; b is 0, 1, 2 or 3; and n is 1 or 2; and the N-oxides, tautomeric forms, stereoisomers and pharmaceutically acceptable salts thereof, and the compound of the general formula I, wherein at least one of the atoms has been replaced by its stable, non-radioactive isotope. 2.-49. (canceled)
 50. A compound of formula I as claimed in claim 1, selected from the group consisting of: 8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolone; 1,2,3,4-tetrahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopent[2]en]-6(7H)-one; 8-methyl-8-phenyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one; 8,8-dimethyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one; 1,2,3,4-tetrahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopentan]-6(7H)-one; 1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopentane]; 12a-methyl-4,5,6,7,10,11,12,12a-octahydrocyclopenta[c][1,4]diazepino[6,7,1-ij]quinolin-9(9aH)-one; 8-methyl-8-(trifluoromethyl)-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolone; 12a-methyl-4,5,6,7,10,11,12,12a-octahydrocyclopenta[c][1,4]diazepino[6,7,1-ij]quinolin-9(9aH)-one; 12a-methyl-4,5,6,7,9,9a, 10,11,12,12a-decahydrocyclopenta[c][1,4]diazepino[6,7,1-ij]quinoline; 8-methyl-8-(trifluoromethyl)-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one; 12a-methyl-4,5,6,7,9,9a, 10,11,12,12a-decahydrocyclopenta[c][1,4]diazepino-[6,7,1-ij]quinoline; 8-methyl-8-phenyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; (R)-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; (S)-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; 9-chloro-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 10-chloro-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 9-chloro-8,8-dimethyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one; 10-chloro-8,8-dimethyl-3,4,7,8-tetrahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-6(2H)-one; 9-fluoro-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 10-fluoro-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclohexane]; 1′,2′,3′,4′,6′,7′-hexahydrospiro[cyclobutane-1,8′-[1,4]diazepino[6,7,1-ij]quinoline; 9′-fluoro-1′,2′,3′,4′,6′,7′-hexahydrospiro[cyclobutane-1,8′-[1,4]diazepino[6,7,1-ij]quinoline]; 7,8,8-trimethyl-1,2,3,4,7,8-hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline]; 9-fluoro-1-methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]; 3-methyl-1′,2′,3′,4′,6′,7′-hexahydrospiro[cyclobutane-1,8′-[1,4]diazepino[6,7,1-ij]quinoline]; 3-benzyl-2′,3′,7′,8′,9′,10′-hexahydro-1H-3′,8′, 10a′-triaza-cyclohepta[de]naphthalene; 2,3,5,6,7,8-Hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-Cyclobutyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-Methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-(Oxetan-3-yl)-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-(Cyclopropylmethyl)-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-(Cyclopentylmethyl)-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; Cyclopropyl(2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxalin-1-yl)methanone; Cyclopentyl(2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxalin-1-yl)methanone; 1-Cyclopropyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-Cyclopentyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-Cyclopropyl-5-methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 6,6-Dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 5,6,7,9,9a, 10,11,12,13,14-decahydro-4H-azepino[1,2-a][1,4]diazepino[1,7,6-de]quinoxaline; 7-Methyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; 1-Fluoro-7-methyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; 1,2,3,4,6,7-Hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopropane]; 4-Methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclopropane]; 11-Fluoro-8,8-Dimethyl-2,3,4,6,7,8-hexahydro-1H-[l 1,4]diazepino[6,7,1-ij]quinoline; 1-Methoxy-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 4,8,8-Trimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 4-Ethyl-8,8-dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 6,8,8-Trimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 8-ethyl-8-methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; (R)-8-ethyl-8-methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; (S)-8-ethyl-8-methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinoline; 4-Methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]; 1-Fluoro-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; 1-Bromo-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; 1-Methyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; 1-Cyclopropyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; 1-Cyclobutyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; 1-Cyclopentyl-5,6,7,9,9a, 10,11,12-octahydro-4H-[1,4]diazepino[1,7,6-de]pyrrolo[1,2-a]quinoxaline; 8-Methyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-8-ol; 8-Methoxy-8-methyl-2,3,4,6,7,8-hexahydro-6H-[1,4]diazepino[6,7,1-ij]quinoline; 2,8-Dimethyl-2,3,4,6,7,8-hexahydro-1H-[1,4]diazepino[6,7,1-ij]quinolin-8-ol; 11-Methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]; 9-Methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]; 4,5,6,7,9,9a,9b,10,10a, 11-Decahydrocyclopropa[3,4]pyrrolo[1,2-a][1,4]diazepino[1,7,6-de]quinoxaline; 1-Ethyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-Propyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-Cyclobutyl-5-methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 5-Methyl-1-(oxetan-3-yl)-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 1-Ethyl-5-methyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 5-Methyl-1-propyl-2,3,5,6,7,8-hexahydro-1H-[1,4]diazepino[1,7,6-de]quinoxaline; 9-Chloro-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]; 10-Methyl-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]; and 10-Chloro-1,2,3,4,6,7-hexahydrospiro[[1,4]diazepino[6,7,1-ij]quinoline-8,1′-cyclobutane]; or a stereoisomer or pharmaceutically acceptable salt thereof.
 51. A pharmaceutical composition comprising a therapeutically effective amount of at least one compound as claimed in claim 1 or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof, or comprising at least one compound as defined in claim 1 wherein at least one of the atoms has been replaced by its stable, non-radioactive isotope in combination with at least one pharmaceutically acceptable carrier and/or auxiliary substance. 52.-54. (canceled)
 55. A method for treating disorders which respond to the modulation of the 5-HT_(2c) receptor, which method comprises administering to a subject in need thereof at least one compound as defined in claim 1 or an N-oxide, a tautomeric form, a stereoisomer or a pharmaceutically acceptable salt thereof.
 56. The method as claimed in claim 55, where the disorders are selected from the group consisting of damage of the central nervous system, disorders of the central nervous system, eating disorders, ocular hypertension, cardiovascular disorders, gastrointestinal disorders and diabetes.
 57. The method as claimed in claim 56, where the disorders are selected from the group consisting of bipolar disorder, depression, atypical depression, mood episodes, adjustment disorders, anxiety, panic disorders, post-traumatic syndrome, psychoses, schizophrenia, cognitive deficits of schizophrenia, memory loss, dementia of aging, Alzheimer's disease, behavioral disorders associated with dementia, social phobia, mental disorders in childhood, attention deficit hyperactivity disorder, organic mental disorders, autism, mutism, disruptive behavior disorder, impulse control disorder, borderline personality disorder, obsessive compulsive disorder, migraine and other conditions associated with cephalic pain or other pain, raised intracranial pressure, seizure disorders, epilepsy, substance use disorders, alcohol abuse, cocaine abuse, tobacco abuse, smoking cessation, sexual dysfunction/erectile dysfunction in males, sexual dysfunction in females, premenstrual syndrome, late luteal phase syndrome, chronic fatigue syndrome, sleep disorders, sleep apnoea, chronic fatigue syndrome, psoriasis, Parkinson's disease, spinal cord injury, trauma, stroke, pain, bladder dysfunction/urinary incontinence, encephalitis, meningitis, eating disorders, obesity, bulimia, weight loss, anorexia nervosa, ocular hypertension, cardiovascular disorders, gastrointestinal disorders, diabetes insipidus, diabetes mellitus, type I diabetes, type II diabetes, type III diabetes, diabetes secondary to pancreatic diseases, diabetes related to steroid use, diabetes complications, hyperglycemia and insulin resistance.
 58. The method as claimed in claim 57, where the disorders are selected from the group consisting of schizophrenia, depression, bipolar disorders, obesity and substance use disorders. 